Improving results of outpatient endometrial biopsies

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study focuses on enhancing the outcomes of outpatient endometrial biopsies performed using the Pipelle device, which is crucial for diagnosing endometrial cancer. The study will identify factors contributing to insufficient sample rates, which can range from 5-23%, and implement strategies to address these issues. Following the interventions, a re-audit of biopsy results will be conducted after six months to assess improvements. The study will take place at Adan Hospital in Kuwait, involving patients undergoing biopsies during a specified timeframe.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* All patients undergoing outpatient endometrial biopsy in the specified time interval (11/2024- 4/2025) will be included.

Exclusion Criteria:

* Could not obtain the sample due to patient physicals, anxiety (patient decline), cervical stenosis, or severe bleeding

Where it's running

• Adan hospital
  Kuwait, Al Ahmadi, Kuwait Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.