Condition: Postmenopausal Women · Intrauterine Diseases · Endometrial Pathology · Sponsor: Faculty of Medicine of Tunis
The goal of this randomized controlled trial is to evaluate the effectiveness of different cervical preparation strategies before office hysteroscopy in postmenopausal women undergoing evaluation for intrauterine pathology. The main questions to answer are: Does cervical preparation improve the success rate of complete office hysteroscopy in postmenopausal women? Which cervical preparation strategy provides better patient tolerance, as assessed by pain intensity during the procedure? Researchers will compare four cervical preparation protocols (14-day vaginal estrogen, 7-day vaginal estrogen, oral misoprostol, and no cervical preparation) to determine their effects on procedural success, pain, procedure duration, and perioperative complications. Participants will be randomly assigned to one of the four cervical preparation protocols. They will undergo office hysteroscopy using a vaginoscopic ("no touch") approach without anesthesia. Then, they will have pain assessed using a visual analog scale (VAS) during the procedure. Finally, these informations will be collected: procedural success, procedure duration, bleeding, and perioperative complications.
This description comes directly from the study's public registry record.
Mohammed Amine Hannachi, Assistant professor · +21699696332 · medaminehannachi3@gmail.com
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| Maternity and neonatology center of Tunis | Tunis, Tunis Governorate, Tunisia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07697781