Intro
Successful implantation of an embryo requires a receptive endometrium, a good quality embryo, and embryoendometrial synchronization in all species ( 1 ).
Endometrial receptivity during the implantation window is often assessed by ultrasonography markers such as
endometrial thickness, echogenic pattern, blood flow, and
biochemical markers ( 2 ). An appropriately thickened endometrium is a crucial factor for embryo implantation and
can predict pregnancy outcome with high sensitivity and
specificity ( 3 ). Moreover, several studies have reported a significant positive correlation between a triple-layered
thickened endometrium of 7 mm (preferably >9 mm) and
pregnancy rate ( 3 - 5 ).
Despite significant advances in ovarian stimulation protocols, treatment of repeated, unresponsive thin endometrium is still a challenge in assisted reproductive cycles,
which usually results in cycle cancellation or repeated implantation failures ( 6 ).
There is a growing body of evidence that the endometrial growth has a relationship with the state of uterine
blood flow ( 2 ). Treatment options, such as low-dose aspirin, oestradiol administration and gonadotropin therapy,
low dose human chorionic gonadotropin (hCG), vitamin
E, pentoxifylline, L-arginine, luteal phase support with
gonadotropin-releasing hormone (GnRH) agonist, intrauterine granulocyte colony-stimulating factor (G-CSF),
vaginal sildenafil, and recent application of stem cell
therapy are suggested for management of a thin lining endometrium ( 7 ).
Sildenafil citrate (Viagra®, Pfizer, NY, USA) is a 5-phosphodiestrase inhibitor that increases smooth muscle relaxation and vasodilation by preventing cGMP breakdown
( 8 ). Sildenafil citrate potentiates uterine blood flow and,
in conjunction with oestrogen, it leads to the oestrogeninduced proliferation of the endometrium ( 9 ).
It has been reported that vaginal sildenafil significantly
reduced peripheral natural killer cell (NK-cell) activity
and improved successful pregnancy rates in women with
histories of recurrent miscarriages. Although the mechanism of influence by sildenafil on natural killer cell activity is unclear, it seems that enhancement of uterine artery
flow has an effective influence on the local endometrial
NK-cell population ( 10 ). However, adverse effects that
include myocardial infarctions and strokes have been associated with this drug in the normal healthy population
( 11 , 12 ).
This comparative pilot study evaluated the effect of
vaginal sildenafil suppositories on endometrial proliferation and IVF outcome in infertile patients with a history
of repeated IVF failure.
Results
During the recruitment process, we enrolled 66 patients and allocated 22 patients to each study group. A
total of 10 patients were lost to follow up for measuring clinical pregnancy for the following reasons: all
of the embryos of their treatment cycle were cryopreserved (n=3), they had no oocytes at retrieval (n=2),
or no embryos to transfer (n=5). The flow diagram explicitly shows the number of participants at the beginning, intervention allocation, follow-up, and analysis
( Fig .1 ).
Table 1 shows the baseline characteristics of the three
study groups. There were no significant differences
among the study groups. The majority of patients had
normal endometrial patterns, which were similar between the three study groups ( Table 1 ). Uterine artery
PI and RI in the left and right were not statistically significant among the study groups (P>0.05). Table 1 shows
the results of the ovulation stimulation cycle and include
initial endometrial thickness, number and type of ampoules used, time interval for ovulation stimulation, and
numbers of total and metaphase II (MII) oocytes. These
parameters did not differ significantly among the three
intervention groups. Table 2 shows numbers of embryos
transferred in total and by grade (A, B and C). These values were not different among the groups. The generated
embryos were graded as good (A and B) or poor (C) according to their morphological features, cleavage stage,
multi-nucleation, equal size blastomeres, and fragmentation rate ( 16 ).
Of note, the embryo transfer days were similar between
the three groups. All of the embryos were transferred either two or three days after ovum pickup.
The endometrial thickness and patterns after the interventions were not statistically different between the
study groups. Additionally, the three intervention groups
were not different in left and right uterine artery PI and
RI. Implantation rate was not statistically significant
over the three groups (P=0.290). Clinical pregnancy
rates were 33.3 (sildenafil), 33.3 (sildenafil+placebo),
and 17.6 (placebo) as seen in Table 2. Although the
clinical pregnancy rates varied among the intervention
groups, they were not statistically different ( Table 3 ).
Vaginal administration of sildenafil had no adverse effects on the patients during the study.
Flowchart of participants in this randomized controlled trials. IVF/ICSI; In vitro fertilization/intracytoplasmic sperm injection and ET; Embryo transfer
Comparison of baseline characteristics and cycle related factors between the sildenafil, sildenafil + placebo, and placebo groups prior to intervention
BMI; Body mass index, PI; Pulsatility index, FSH; Follicle stimulating hormone, LH; Luteinizing hormone, RI; Resistance index, and MII; Mature metaphase II.
Comparison of treatment cycle outcomes between the sildenafil, sildenafil+placebo, and placebo groups after intervention
PI; Pulsatility index, RI; Resistance index, and ET; Embryo transfer.
Comparison of reproductive outcomes between the sildenafil, sildenafil+placebo, and placebo groups after intervention
Data are presented as n (%).
Discussion
The importance of the endometrial pattern as a predictor
of treatment cycle outcome in IVF-treated patients is
well-documented ( 17 ). In addition, endometrial quality is
also an important factor for the successful implantation
of the foetus ( 18 ). Endometrial thickness increases with
high pregnancy rates; however, pregnancy rates are not
predictable only based on endometrial thickness ( 19 ).
Uterine arterial blood flow seems to affect endometrial
growth and the outcome of pregnancy. Studies have shown
that sildenafil widens the vasculature by its effects on the
smooth muscles of the arteries ( 10 , 20 ). Sildenafil citrate
is an inhibitor-5-phosphodiestrase type that, by preventing
the effect of cGMP, exacerbates the effect of NO on the
smooth muscle of the arteries ( 20 , 21 ). According to the
results of some studies, the use of sildenafil during the
proliferative phase of the cycle improves uterine blood
flow and endometrial growth, and results in a higher
level of implantation and pregnancy in patients with
repeated IVF failure and Ashermen syndrome ( 8 , 22 ).
Also the administration of sildenafil (50 mg intravenous)
in a sterilized animal model (sheep) has been shown to
exacerbate uterine flow ( 23 ). Several studies have shown
a correlation between ‘‘thin endometrium’’ and low
implantation rates ( 9 , 24 ). The results of current study
showed increased endometrial thickness in the three
groups on the day of hCG injection, but the increase
was not statistically significant. The results of previous
studies have shown that sildenafil citrate (vaginal or
oral alone or with oestradiol) is significantly effective in
improving endometrial thickness ( 25 - 27 ). Sher and Fisch
( 22 ) reported that the use of sildenafil vaginal suppository
could reduce the adverse effects of headache and low
blood pressure compared with oral sildenafil. In another
study, they reported that vaginal sildenafil (25 mg, 4 times
per day) improved endometrial thickness (≥9 mm) in
70% of the patients ( 8 ). In a prospective study, Takasaki
et al. ( 25 ) compared the effects of vaginal vitamin E,
L-arginine, and vaginal sildenafil citrate on endometrial
thickness in patients with endometrial thickness less than
8 mm and right arterial resistance in their radial vessels
(RA-RI ≥0.81). The results showed that vitamin E,
L-arginine, and sildenafil citrate significantly improved
RA-RI and endometrial thickness in these patients;
however, the improvement in endometrial thickness in
patients treated with sildenafil citrate was more than the
other two groups. Several studies ( 26 - 28 ) showed that
vaginal sildenafil significantly improved endometrial
thickness in patients with history of poor endometrial
thickness in the previous cycles. Jerzak et al. ( 10 ) reported
that endometrial thickness significantly increased after
administration of oral sildenafil (25 mg, 4 times per day) in
women with a history of abortion. Dehghani Firouzabadi
et al. ( 29 ) recommended oral sildenafil administration
as an appropriate solution for improving endometrial
admission in patients with unsuccessful cycles from
low endometrial thickness. Their results showed that the
triple line endometrial pattern in the sildenafil citrate +
oestradiol group was significantly higher than in the
oestradiol-only group, while the intermediate pattern of
the endometrium was not significantly different between
the two groups. Fetih et al. ( 30 ) reported that sildenafil
vaginal gel significantly increased endometrial thickness
and uterine blood flow, and might improve pregnancy rate
in patients with clomiphene citrate (CC) failure due to
thin endometrium. The results reported by Chanona et al.
( 31 ) showed that the use of vaginal sildenafil in patients
whose endometrial thickness was equal to or less than 7
mm in the failed assisted reproductive technology (ART)
cycles led to an increase in implantation and pregnancy.
Zinger et al. ( 32 ) reported that two patients with a history
of curettage and secondary infertility were treated with
sildenafil after removing adhesions by surgery (due to thin
endometrial thickness in previous IVF cycles), and both
patients became pregnant during the first cycle of sildenafil
administration. Increases in their endometrial thicknesses
was also shown in transvaginal ultrasonography.
Several treatment modalities have been offered to
patients with ‘‘thin’’ endometrium, including hormonal
manipulation by oestrogen and gonadotropin therapy,
low-dose hCG, tamoxifen, L-arginine or sildenafil,
vitamin E, pentoxifylline, low-dose aspirin, hysteroscopic
adhesiolysis, intrauterine infusion of growth factor such
as G-CSF, and the recent application of regenerative
medicine. Despite the large variety of treatment,
most options lead to only minor modifications in the
endometrium thickness and subsequent pregnancy,
and when this modality fails, patients are eventually
candidates for surrogacy. Treatment of thin endometrium
remains a challenge and future investigations are required
to further clarify and ideally manage patients with thin
endometrium ( 7 ).
In the present study, the clinical and chemical
pregnancy rates in the two groups of women who were
taking sildenafil alone and the women who took placebo and sildenafil showed a twofold increase compared to
the placebo-only-treated women, which according to the
sample size, this increase is not significant. The results
reported by Dehghani Firouzabadi et al. ( 29 ) in a study of
80 patients showed that the chemical pregnancy rate was
higher but not statistically significant in the patients who
used sildenafil; this finding was consistent with the results
of our study. However, AbdelKader Fahmy et al. ( 33 ),
with a sample size of 70 patients, reported a significantly
greater chemical pregnancy rate in the sildenafil group.
In this study, the clinical pregnancy rate was higher in
the sildenafil and sildenafil+placebo groups than in the
placebo group. Although this increase was not statistically
significant, it was clinically shown to be twofold. These
results were consistent with the findings of AbdelKader
Fahmy et al. ( 33 ) and Kim et al. ( 28 ). The study by
AbdelKader Fahmy et al. ( 33 ) reported a 2.5-fold increase
in pregnancy in the sildenafil group, but this difference
was not statistically significant. Kim et al. ( 28 ) reported
that the use of vaginal sildenafil plus oral oestrogen pills
in the luteal phase of patients treated with an IVF-ET cycle
increased the pregnancy rate by two-fold, but this increase
was not statistically significant. Mangal and Mehirishi
( 34 ) showed that the rate of pregnancy in the patients who
used vaginal sildenafil in three successive intra uterine
insemination (IUI) cycles was significantly higher in the
third cycle than in the group who used oestradiol valerate,
while this difference was not significant in the first and
second cycles. The findings from a retrospective study by
Margreiter et al. ( 35 ) showed a significant improvement
in the rate of implantation, endometrial thickness and
pregnancy, and decreased abortion in the group of patients
treated with vaginal sildenafil.
The endometrial receptivity is an important stage
in the ART cycles, the results of our study showed
a higher rate of implantation in the women who took
sildenafil+placebo than in the other two groups, which
was consistent with the results of Dehghani Firouzabadi
et al. ( 29 ).
In the present study, 2 out of 7 cases of pregnancy
ended in abortion in the sildenafil group, 1 out of 6 cases
of pregnancy in the sildenafil+placebo group, and 0 of
3 cases of pregnancy in the placebo group. The rate of
abortion was negligible in the sildenafil group. Follow-up
evaluations showed a molar pregnancy in the sildenafil
group. Dzieciol et al. ( 36 ) reported that sildenafil citrate
increased uterine tissue perforation during the uterus
preparation for fertility.
In our study, higher numbers of MII oocytes were
retrieved in the sildenafil groups compared to the
placebo group, which was clinically important; however,
one-way ANOVA results showed that this finding was
not statistically significant. To our knowledge, there
is only one study (abstract available) by Vidal et al.
( 37 ) that provided evidence of the benefit of sildenafil
supplementation in the first days of hyperstimulation
induction in terms of the numbers of mature and fertilized
oocytes. Therefore, more research on this topic needs to
be undertaken.
Conclusions
Vaginal sildenafil might conceivably improve chemical
and clinical pregnancy rates in repeated IVF failure
patients. Since this was a pilot study, we recommend that
clinical trials should be conducted with vaginal or oral
sildenafil on larger numbers of these patients.
Materials Methods
This phase II randomized, double-blind, placebo-controlled trial was performed at Royan Institute, Reproductive
Biomedicine Research Center, Tehran, Iran, between February 14, 2014 and November 14, 2016 ( NCT03192709 ).
The assessors and patients were not aware of the treatment
allocated. The Institutional Review Board and Ethics Committee of Royan Institute, Tehran, Iran reviewed and approved this study in compliance with the Declaration of
Helsinki (EC/88/1045). Informed consent was obtained
from all patients prior to their participation in the study.
The study population consisted of 66 infertile women
aged ≤38 years. The inclusion criteria was met when the
women had normal ovarian reserve [blood anti-mullerian
hormone (AMH) levels >1.5 ng/mL] with at least two
prior cycles with follicle stimulating hormone (FSH) <10
mIU/ml; a history of two prior consecutive failed IVF/
ICSI attempts with at least a transfer of two good quality fresh or frozen-thawed embryos; hCG day endometrial thickness <7 mm in all prior IVF/ICSI attempts; and
normal endometrial appearance according to either hysterosonography, hysterosalpingography, or hysteroscopy.
Women were excluded if they had a history of myomectomy or Asherman’s syndrome.
A preliminary colour Doppler transvaginal sonography
with a 4-8 MHz probe (ProSound Alpha 10; Aloka, Japan) was performed by an expert radiologist on day 14
of the patient’s prior menstrual cycle to investigate the
uterine and adenexes for any abnormal findings. The endometrial parameters of endometrial thickness, endometrial pattern, pulsatility index (PI), and resistance index
(RI) were measured. The uterine artery PI and RI were
obtained through flow velocity waveforms from the ascending branch of the uterine artery at the point near to
the internal cervical orifice and calculated as previously
described ( 13 ). In the subsequent cycle, ovarian stimulation was performed with the long protocol using a GnRH
agonist ( 14 ).
In the IVF treatment cycle, the patients were randomly
assigned to three groups according to a random allocation sequence generated by a randomized block design.
The size of each block was 3. In group A, the sildenafil
(vaginal suppositories, 100 mg/day, Parnian Daroo, Co.,
Tehran, Iran) were administered from the first day of the
FSH injection until the day of oocyte retrieval. In group
B, placebo (vaginal suppositories, Parnian Daroo, Co.,
Tehran, Iran) was initiated from the first day of the HMG
injection until 2 days before the hCG injection, after
which sildenafil vaginal suppositories were initiated and
continued until the day of oocyte retrieval. In group C, the
placebo was given from the first day of HMG injection
until the day of oocyte retrieval. Participants received 10
000 IU of hCG (Choriomon, IBSA, Switzerland) when
at least two dominant follicles were 18 mm in diameter.
Endometrial thickness, pattern, PI and RI were measured
on the day of hCG administration and compared with the
data obtained in the previous cycle without sildenafil citrate treatment. Oocytes were retrieved 36 hours later via
transvaginal ultrasound-guided needle aspiration.
Embryo transfer was performed after 48 hours of oocyte retrieval. Progesterone in oil (100 mg, IM daily) or
intravaginal progesterone (400 mg, twice daily) was used
for luteal support and maintained until the pregnancy test
was conducted. Serum hCG levels were measured on the
14 th day following oocyte retrieval. Vaginal ultrasound
confirmation of pregnancy was performed at 4-6 weeks
after embryo transfer.
A chemical pregnancy was determined by a positive
ß-hCG test result. A clinical pregnancy was confirmed
by ultrasonography visualization of one or more gestational sacs or definitive clinical signs of pregnancy.
The spontaneous abortion was defined as a pregnancy loss of an intrauterine pregnancy before 22 weeks’ gestation ( 15 ).
Suppositories containing 100 mg of sildenafil were
prepared from the oral tablets by a local pharmacy (Parnian Daroo, Iran). We defined the endometrial thickness
threshold cut-off of <7 mm as a thin endometrium based
on other studies ( 8 ).
Data are expressed as mean ± standard error (SE)
and proportion. Continuous and categorical outcome
variables were compared between three intervention
groups by one-way analysis of variance (ANOVA)
and the chi-square test. All statistical analyses were
performed using SPSS version 22 for Windows 7
(IBM Analytics, Armonk, NY). The significance level
was set at 0.05.
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