Predictive Factors for Successful Operative Hysteroscopy Using Tissue Removal Device (TruClear System) Without Anesthesia

Retained Products of Conception Clinical Trial

Official title:
Predictive Factors for Successful Operative Hysteroscopy Using Tissue Removal Device (TruClear System) Without Anesthesia

Status Recruiting

Clinical Trial Summary

Background: Small-diameter operative hysteroscopes may allow to perform operative hysteroscopy without general anesthesia in selected patients. One of these instruments is the tissue removal device (TRD), which resects and removes intrauterine pathology such as endometrial polyps and retained products of conception (RPOC) with a diameter of ¬6 mm. Objective: To assess the success rate and intraoperative pain of patients undergoing operative hysteroscopy without anesthesia with the TRD (TruClear Elite Mini-Hysteroscope) for removal of endometrial polyps or RPOC. Methods: Prospective observational study. Participation in the study was offered to patients diagnosed with uterine polyps or RPOC on office diagnostic hysteroscopy. The patients filled out a digital questionnaire before and after the operation. A successful procedure was defined as complete hysteroscopic removal of the uterine pathology using the TruClear system. Oral 400 mcg misoprostol 12 hours before the procedure was prescribed for cervical ripening.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Retained Products of Conception

Clinical Trial Details

NCT number	NCT05722028
Study type	Observational
Source	Assaf-Harofeh Medical Center
Contact	Noam Smorgick, Prof
Phone	+97289542512
Email	nsmorgik@shamir.gov.il
Status	Recruiting
Phase
Start date	August 1, 2022
Completion date	August 31, 2023

View Details

See also
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