Methods
We conducted a prospective, randomized, double-blind, placebo-controlled clinical trial. Patients received a standard dose of topical ropivacaine (injected at the three portal sites and atomized in the abdominal cavity) or placebo. The primary outcome was the evaluation of post-operative pain intensity 6 h after surgery. Secondary outcomes included the intensity of pain during the 48 h after surgery, shoulder tip pain and the request for rescue analgesics during the first 48 h after surgery, time to discharge from recovery room, time to mobilizing on the ward and time to return to daily activities. Patients were divided in two groups (Group_A: benign adnexal pathologies; Group_B: benign uterine diseases) and assigned to Subgroup_1 (receiving ropivacaine) and Subgroup_2 (receiving placebo).
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Acknowledgments
The authors thank the whole staff of Gynecological and Obstetrics Clinical Unit (Department of Woman and Child Health) that participated to data collection and to the study realization.
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Carlo Saccardi, Salvatore Gizzo, Amerigo Vitagliano, Marco Noventa, Masimo Micaglio, Matteo Parotto, Mauro Fiorese, Pietro Litta have no conflicts of interest or financial ties to disclose.
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Saccardi, C., Gizzo, S., Vitagliano, A. et al. Peri-incisional and intraperitoneal ropivacaine administration: a new effective tool in pain control after laparoscopic surgery in gynecology: a randomized controlled clinical trial. Surg Endosc 30, 5310–5318 (2016). https://doi.org/10.1007/s00464-016-4881-2
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DOI: https://doi.org/10.1007/s00464-016-4881-2