Comparison of the incidence of inadequate tissue sampling from uterine curettage in abnormal uterine bleeding between standard and transabdominal ultrasound guided procedure

Phase 3

• Conditions: endometrial sampling; Inadequae tissue; Inadequate tissue, abnormal uterine bleeding, ultrasound guided&#44

• Registration Number: TCTR20191211001
• Lead Sponsor: donthani hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-12-11
• Study Completion: 2020-08-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: Female
• Target Recruitment: 144

Inclusion Criteria

Woman age > 35 years with abnormal uterine bleeding

Exclusion Criteria

No inform consent, pregnancy, pethidine or analgesic allergy, arrythmia, abnormal sensation, genitourinary neoplasms, coagulopathy, lower urinary tract infection, pelvic inflammatory disease

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Decrease inadequate tissue in ultrasound guided group Admission time until endometrial sampling Pathology results

Secondary Outcome Measures

Name	Time	Method
Duration of procedure Between Apply and off the speculum Time