efficacy of Ibuprofen and paracetamol in reducing pain after endometrial biopsy in abnormal uterine bleeding women at gynecologic-outpatient department of sunprasitthiprasong hospital

Phase 2

Recruiting

• Conditions: All women who have abnormal uterine bleeding; Abnormal uterine bleeding

• Registration Number: TCTR20231017005
• Lead Sponsor: no

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-10-17
• Study Completion: 2023-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 98

Inclusion Criteria

Abnormal uterine bleeding women with 1. age more than 35 years old or 2.risk for anovulation (PCOS, BMI more than 25 kg/m2, abnormal ultrasound finding) or 3. medical failure treatment or 4.risk of endometrial cancer (Tamoxifen using, Lynch syndrome, family history of colon or cervical cancer)

Exclusion Criteria

1. do not consent to participate
2. pregnancy
3. History of allergy or suspected allergy of Paracetamol or Ibuprofen
4. Asthma, GI bleeding, liver disease, renal disease, cardiovascular disease

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain score at 30 minutes after the procedure 30 minutes after the procedure Numeric rating scale

Secondary Outcome Measures

Name	Time	Method
pain score during the procedure 30 minutes after the procedure Numeric rating scale,pain score at immediately after the procedure immediately after the procedure Numeric rating scale,pain score at 60 minutes after the procedure 60 minutes after the procedure Numeric rating scale,satisfactation 30 minutes after the procedure less, intermediate, very statisfied