Clinical Trial

Pipelle Versus Karman Endometrial Biopsy Under Standardized Paracervical Block

Study acronym: PB-EMB
Completed
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Summary
Endometrial biopsy is a commonly used outpatient procedure to evaluate abnormal uterine bleeding and postmenopausal bleeding. Different sampling methods are available, but their diagnostic adequacy and patient experience may vary. This prospective randomized study compares two commonly used endometrial biopsy methods, Pipelle and Karman cannula, under standardized paracervical block anesthesia. All participants receive the same local anesthetic technique to minimize pain-related differences between methods. The primary objective is to compare the rate of clinically adequate endometrial samples obtained with each method. Secondary outcomes include patient-reported pain, patient satisfaction, procedure duration, need for additional diagnostic procedures, and hospital-related costs. Study findings are expected to support clinical decision-making regarding the most effective and practical endometrial biopsy method when adequate pain control is provided.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2026-01-16; most recent amendment 2026-02-09.
Status change: Recruiting → Completed 2026-02-09
Trial Details
NCT Number NCT07366814
Lead Sponsor Gaziosmanpasa Research and Education Hospital
Conditions Abnormal Uterine Bleeding, Postmenopausal Bleeding
Enrollment 480 participants
Start Date 2026-01-03
Primary Completion 2026-01-31 (estimated)
Study Completion 2026-02-09 (estimated)
Updated on ClinicalTrials.gov 2026-02-10