Abstract
Background: Female infertility is a multifactorial condition with variable etiological patterns that differ
across populations. Identifying specific causes is essential for accurate diagnosis and targeted management.
Material and methods
A cross-sectional study was conducted among 120 infertile women attending a
tertiary-care gynaecology outpatient department. Detailed clinical evaluation, hormonal profiling,
ultrasonography and diagnostic hystero-laparoscopy were performed to determine etiological factors.
Results
Ovarian causes were most prevalent (50%), followed by tubal (22.5%), uterine (20%), peritoneal
(18.3%) and unexplained infertility (20%). Laparoscopic evaluation enhanced diagnostic clarity, revealing
a high burden of ovarian abnorm alities, tubal blockages and peritoneal pathology including endometriosis
and pelvic adhesions.
Conclusion
Infertility in this population demonstrated a heterogeneous etiological distribution dominated
by ovarian, tubal and peritoneal factors. Comprehensi ve diagnostic evaluation is essential for
individualized management and improved reproductive outcomes.
Keywords
Infertility, tubal factor, laparoscopy, ovarian dysfunction
Introduction
Infertility, defined as the inability to conceive after 12 months of regular unprotected
intercourse, remains a significant global reproductive health issue affecting millions of couples.
Recent estimates indicate that the worldwide 12 -month prevalence of infertility is approximately
17.5%, reflecting a substantial burd en on healthcare systems and families alike [1]. Global
analyses from 1990 -2021 further show a rising trend in female -specific infertility, with notable
regional variations driven by socioeconomic, environmental, and healthcare -access differences
[2].
Female infertility arises from a diverse spectrum of etiological factors, including ovulatory
disorders, tubal pathology, uterine abnormalities, endometriosis, endocrine dysfunction,
infections, and unexplained causes. Studies have demonstrated that ovulatory dysfunctions
particularly polycystic ovary syndrome (PCOS) are among the most common contributors to
female infertility worldwide [3]. In addition, tubal factor infertility remains highly prevalent,
especially in low - and middle -income countries where pelv ic inflammatory disease (PID),
genital tuberculosis, and sexually transmitted infections continue to influence reproductive
morbidity [4].
Uterine causes such as fibroids, intrauterine adhesions, and congenital anomalies also play a
significant role in pre venting implantation or sustaining early pregnancy [5]. Endometriosis an
inflammatory, estrogen-dependent condition can impair fertility through altered pelvic anatomy,
chronic inflammation, and reduced ovarian reserve, affecting approximately 10% of
reproductive-age women and nearly 50% of infertile women in some populations [6].
Notably, age has emerged as one of the strongest predictors of female fertility potential. A
tertiary-care based analysis highlighted a steep decline in ovarian reserve and oocyte quality
beyond the age of 35, significantly increasing the likelihood of infertility and need for assisted
reproductive technologies [7]. Lifestyle -related factors such as obesity, smoking, stress,
environmental endocrine disruptors, and delayed childbear ing have further compounded
infertility rates in modern populations [8].
While global and regional data are widely available, etiological patterns often differ significantly
across countries and within different levels of healthcare facilities. A 2023 tert iary-care study
from Asia reported ovulatory disorders as the leading cause, followed by tubal factor infertility,
International Journal of Clinical Obstetrics and Gynaecology https://www.gynaecologyjournal.com
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endometriosis, and unexplained infertility, underscoring the need
for local data to guide clinical services [9]. Another multi -
institutional study emphasized that accurate identification of
female-factor infertility improves diagnostic precision, ensures
appropriate referrals, and enhances treatment outcomes
especially in resource-limited settings [10].
Given the variability in etiological f actors and the influence of
regional health dynamics, there is a need for updated, institution-
specific data on the incidence and distribution of various causes
of female infertility. Therefore, the present study aims to
evaluate the incidence of different causes of infertility among
women attending the gynaecology outpatient department (OPD)
of a tertiary-care centre, helping to guide targeted diagnostic and
management strategies for optimal reproductive outcomes.
Material and methods
This hospital -based observational study was conducted in the
Department of Obstetrics and Gynaecology at a tertiary care
centre over a defined study period. A total of 120 women
presenting to the gynaecology outpatient department (OPD) with
complaints of infertility were incl uded. Infertility was defined as
the inability to conceive after at least 12 months of regular
unprotected intercourse. Both primary and secondary infertility
cases were enrolled after obtaining written informed consent.
All eligible participants underwent detailed history taking,
clinical examination, and appropriate investigations to identify
etiological factors contributing to infertility. History included
age, duration of infertility, menstrual pattern, obstetric history,
medical and surgical history, p rior pelvic infections,
contraceptive use, lifestyle factors and previous treatment for
infertility. Clinical examination involved general physical
assessment, body mass index calculation, and systemic
examination with emphasis on thyroid, breast and pelvi c
evaluation.
Investigations were performed according to standardized
departmental protocols. Ovulatory function was assessed
through menstrual history, mid -luteal serum progesterone where
necessary, and ultrasonographic evaluation of follicular
development. Hormonal assays including thyroid -stimulating
hormone (TSH), prolactin and, when indicated, serum androgens
and anti -Müllerian hormone (AMH) were obtained. Pelvic
ultrasonography was performed to identify ovarian morphology,
uterine anomalies, endometrial thickness and adnexal pathology.
Tubal patency was evaluated through hysterosalpingography
(HSG), and laparoscopy was advised in selected cases where
endometriosis, adhesions or tubal pathology required further
confirmation. Uterine cavity abnormalities were assessed using
transvaginal sonography and diagnostic hysteroscopy when
required.
Based on clinical findings and investigation results, the causes of
infertility were categorised into ovulatory dysfunction, tubal
factor, uterine factor, endometriosis, cervical factor, unexplained
infertility, or mixed causes. Each participant was classified
under the predominant etiological category.
All collected data were systematically recorded in a predesigned
proforma and subsequently entered into a spreadsheet f or
analysis. Statistical analysis was performed using appropriate
software. Descriptive statistics including frequency distribution
and percentages were computed to determine the incidence of
different causes of infertility within the study population.
Results
were presented in tables and charts wherever applicable.
Ethical approval was obtained from the institutional ethics
committee prior to the commencement of the study.
Results
A total of 120 women with infertility were included in the
present study. O f these, 74 women (61.6%) presented with
primary infertility and 46 women (38.4%) with secondary
infertility. The distribution of etiological factors showed
considerable overlap between the two groups, although certain
patterns emerged on detailed evaluati on. As shown in Table 1,
ovarian factor infertility constituted the largest category overall,
affecting half of the study population. Among women with
primary infertility, 54.05% exhibited ovarian dysfunction,
whereas 43.47% of secondary infertility cases were attributed to
ovarian causes. Tubal factor infertility accounted for 22.5% of
all cases, with a relatively similar distribution between primary
and secondary infertility. Uterine factor infertility contributed to
20% of cases, whereas peritoneal facto rs such as endometriosis,
adhesions and pelvic pathology were responsible for 18%.
Unexplained infertility continued to represent a significant
proportion and was more common among secondary infertility
patients at 28.26%, compared to 14.86% in primary infertility.
Laparoscopic evaluation was performed in 94 women (78.3%),
providing detailed information on intra -abdominal and pelvic
pathology. The findings are presented in Table 2. Ovarian
abnormalities were the most frequently detected pathology,
identified in 40.42% of women who underwent laparoscopy.
Polycystic ovarian morphology constituted the majority of
ovarian findings and was more frequently observed among those
with primary infertility. Tubal blockage was noted in 22.34% of
cases, including bilater al block, unilateral block and
hydrosalpinx. Peritoneal causes such as endometriosis, pelvic
adhesions and genital tuberculosis contributed significantly to
primary infertility, accounting for 25.53% of laparoscopic
findings. Uterine pathology including fi broids, müllerian
anomalies and hypoplastic uterus represented 11.7% of
abnormalities.
Hystero-laparoscopic correlation of etiological factors is
summarized in Table 3. Ovarian factors remained the
predominant cause (38.29%), followed by tubal factors (27.65%)
and peritoneal factors (24.46%). Uterine causes contributed to
25.53% of cases, while unexplained infertility accounted for
22.34% of the evaluated women. This combined evaluation
strengthened the diagnostic precision and highlighted the
multifactorial nature of infertility among the study participants.
Table 1: Causes of infertility (N = 120)
Causes of infertility Primary (N=74) Number Primary % Secondary (N=46) Number Secondary % Total (N=120) Number Total %
Ovarian factor 40 54.05 20 43.47 60 50.00
Tubal factor 17 22.97 10 21.73 27 22.50
Uterine factor 15 20.27 9 19.56 24 20.00
Peritoneal factor 15 20.27 7 15.21 22 18.33
Unexplained 11 14.86 13 28.26 24 20.00
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Table 2: Laparoscopically identified pathology of infertility (N = 94)
Causes of infertility Primary (N=58) Frequency (%) Secondary (N=36) Frequency (%) Total (N=94) Frequency (%)
Ovarian factor
PCOS 14 (24.13) 7 (19.44) 21 (22.34)
Simple cyst 1 (1.72) 1 (2.78) 2 (2.12)
Chocolate cyst 5 (8.62) 1 (2.78) 6 (6.38)
Complex cyst 5 (8.62) 1 (2.78) 6 (6.38)
Streak ovaries 1 (1.72) 0 1 (1.06)
Total ovarian 26 (44.82) 10 (27.78) 38 (40.42)
Tubal factor
Bilateral block 9 (15.51) 3 (8.33) 12 (12.76)
Unilateral block 3 (5.17) 6 (16.67) 9 (9.57)
Hydrosalpinx 0 2 (5.56) 2 (2.12)
Total tubal 12 (20.68) 11 (30.56) 23 (24.46)
Uterine factor
Fibroid 3 (5.17) 2 (5.56) 5 (5.31)
Mullerian anomaly 2 (3.44) 1 (2.78) 3 (3.19)
Hypoplastic uterus 1 (1.72) 0 1 (1.06)
Total uterine 6 (10.34) 3 (8.33) 9 (9.57)
Peritoneal factor
Endometriosis 5 (8.62) 4 (11.11) 9 (9.57)
Pelvic adhesions 4 (6.89) 2 (5.56) 6 (6.38)
Tuberculosis 5 (8.62) 0 5 (5.31)
Total peritoneal 14 (24.13) 6 (16.67) 20 (21.27)
Table 3: Hystero-laparoscopically identified causative factors of infertility (N = 94)
Causes of infertility Primary (N=58) Number Primary % Secondary (N=36) Number Secondary % Total (N=94) Number Total %
Uterine factor 15 25.86 8 22.22 23 24.46
Tubal factor 15 25.86 11 30.56 26 27.65
Ovarian factor 26 44.82 10 27.78 36 38.29
Peritoneal factor 14 24.13 6 16.67 20 21.27
Unexplained 11 18.96 10 27.78 21 22.34
Discussion
The present study examined the distribution of
etiological factors contributing to infertility among women
attending a tertiary-care gynaecology outpatient department. The
findings reaffirm the multifactorial nature of infertility, with
ovarian, tubal, uterine and peritoneal pathologies contributing
substantially to both primary and secondary infertility. Ovarian
dysfunction emerged as the leading cause, consistent with global
evidence showing that ovulatory disorders particularly PCOS
remain the most frequent contributor to female infertility in
reproductive-age women [11]. In recent literature, ovulatory
dysfunction has been closely associated with metabolic
disturbances, chroni c anovulation and endocrine dysregulation,
which collectively impair fecundity and contribute to the rising
burden of infertility in younger age groups [12].
Tubal factor infertility accounted for more than one -fourth of
cases on combined hystero-laparoscopic evaluation. This finding
aligns with contemporary studies demonstrating that tubal
pathology continues to be a major cause of infertility, especially
in populations with high prevalence of pelvic inflammatory
disease, post -infectious sequelae and delay in seeking
gynecological care [13]. Laparoscopic assessment remains the
gold standard for accurate identification of tubal blockages,
hydrosalpinx and peritubal adhesions, as imaging alone
frequently underestimates the extent of tubal damage.
Peritoneal causes including endometriosis, pelvic adhesions and
genital tuberculosis were also significant contributors.
Endometriosis, identified in nearly 10% of women, is known to
reduce fecundity through a combination of pelvic inflammation,
altered immunologic en vironment and mechanical distortion of
pelvic structures. Recent evidence emphasizes that even
minimal-to-mild endometriosis significantly affects reproductive
potential and requires targeted management to improve
conception rates [14]. Genital tuberculosi s, although less frequent
globally, remains a notable contributor in South Asian
populations, and its diagnosis is frequently delayed due to subtle
or absent clinical symptoms.
Uterine factors such as fibroids, congenital malformations and
hypoplastic uter us accounted for over 20% of cases in the
present study. According to recent literature, uterine anomalies
demonstrate varying degrees of impact on fertility depending on
the location, size and distortion of the endometrial cavity [15].
Fibroids impinging upon the cavity, in particular, are associated
with implantation failure and increased miscarriage risk.
Unexplained infertility constituted a considerable proportion of
cases, especially among secondary infertility patients. This
category reflects the lim itations of current diagnostic modalities
and the complex interplay of endometrial receptivity,
immunological factors and subtle ovulatory defects. As
emphasized in recent reviews, unexplained infertility
underscores the need for advanced diagnostic tools and
individualized treatment approaches [12].
Overall, the findings of this study resonate with recent global
trends indicating that infertility remains a heterogeneous
condition requiring comprehensive evaluation. The integration
of clinical assessment, h ormonal profiling, transvaginal
ultrasonography and diagnostic laparoscopy improves diagnostic
accuracy and allows for targeted management. The high
proportion of ovarian and tubal pathology in this population
highlights the importance of early detection, lifestyle
modification, infection prevention strategies and timely referral
to specialized infertility services.
Conclusion
Female infertility in this tertiary -care population
was predominantly attributed to ovarian, tubal and peritoneal
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factors, with a noticeable contribution from uterine
abnormalities and unexplained causes. Laparoscopic evaluation
significantly enhanced diagnostic precision, identifying multiple
coexisting pathologies not detectable through routine imaging.
These findings highlight the complex and multifactorial nature
of infertility and emphasize the need for early, comprehensive,
and individualized evaluation. Strengthening diagnostic facilities
and awareness among reproductive -age women may improve
fertility outcomes and reduce long-term reproductive morbidity.
Conflict of interest: No! Conflict of interest is found
elsewhere considering this work.
Source of Funding: T here was no financial support
concerning this work
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How to Cite This Article
Dr. Patel PD, Dr. Londhe P, Dr. Gadhvi MH. Investigating the contributors
to female infertility: A comprehensive study . International Journal of
Clinical Obstetrics and Gynaecology 2025;9(6):974-977.
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