Does the anesthetic method during endometrial sampling affect sexual function a month later?
Official title: Evaluation of One-Month Female Sexual Function Index (FSFI) Scores in Women Undergoing Endometrial Sampling Under Sedo-Analgesia Versus Local Anesthesia
Run by Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization · NCT07628660 · Data updated 2026-11-12
This study tests whether sedo-analgesia or local anesthesia during endometrial sampling influences female sexual function one month after the procedure.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | Women only |
| Enrollment | 210 (estimated) |
| Sponsor | Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization Academic / other |
| Locations | 1 site (Istanbul) |
| Status | Recruiting |
| Started | April 15, 2026 |
| Main results expected | May 15, 2027 |
| Study ends | May 15, 2027 |
| Registry record updated | June 5, 2026 |
| Trial ID | NCT07628660 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women aged 18–60 undergoing endometrial sampling at Prof. Dr. Cemil Taşcıoğlu City Hospital and able to complete the FSFI at 1 month.
✕Probably not a fit
Participants who do not experience changes in sexual function or who miss the 1-month follow-up may see no direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective observational study compares FSFI scores one month after endometrial sampling performed under either sedo-analgesia or local anesthesia. 210 women aged 18 to 60 undergoing routine endometrial sampling at a single hospital will be grouped by the anesthesia technique used. FSFI questionnaires collected at the 1-month follow-up will be analyzed to see if anesthesia type is associated with differences in sexual function, with secondary context on pain and discomfort. The study aims to provide insight into whether anesthesia choice during the procedure has short-term effects on sexual well-being. Enrollment is planned from April 2026 to April 2027 at Prof. Dr. Cemil Taşcıoğlu City Hospital.
Why it matters
Potential benefit: If a difference is found, anesthesia choice could be informed to minimize potential negative effects on sexual function after endometrial sampling.
How similar studies have gone: There is limited prior data on how anesthetic technique during gynecologic procedures affects subsequent sexual function, making this study relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female patients aged 18 to 60 years * Undergoing endometrial sampling at the Department of Obstetrics and Gynecology, Prof. Dr. Cemil Taşcıoğlu City Hospital * Undergoing the procedure under sedo-analgesia or local anesthesia as part of routine clinical practice * Attendance at the 1-month follow-up visit * Ability to complete the Female Sexual Function Index (FSFI) questionnaire Exclusion Criteria: * Age younger than 18 years or older than 60 years * Presence of known chronic systemic disease * Incomplete clinical or follow-up data * Failure to attend the 1-month follow-up visit * Inability or unwillingness to complete the FSFI questionnaire
Where it's running
-
Prof.Dr.Cemil Taşcıoğlu City Hospital
Istanbul, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Yağmur ÖZKAN, M.D.
- Email: yagmurolmez92@hotmail.com
- Phone: +90 5374318241
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.