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To compare the effects of two drugs in the management of abnormal uterine bleeding

Not Applicable
Conditions
Health Condition 1: N938- Other specified abnormal uterine and vaginal bleeding
Registration Number
CTRI/2024/07/070066
Lead Sponsor
Government Medical College and Hospital Sector Chandigarh India Pincode
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Women presenting to Gynaecological OPD with Abnormal Uterine Bleeding related to structural causes of the uterus, uterine fibroids and adenomyosis

Exclusion Criteria

1. Women with bulky fibroids presenting with pressure symptoms who are not fit for medical management.

2. Submucosal fibroid type 0 and type 1.

3. Endometrial polyp, endometrial hyperplasia or malignancy.

4. Complex adnexal mass.

5. Acute AUB.

6. Abnormal renal or hepatic function tests.

7. Coagulopathy.

8. History of breast or genital malignancy.

9. Smoking.

10. Thromboembolic disease.

11. Diabetes, hypertension, migraine or epilepsy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in amount and duration of menstrual blood loss by assessing pattern of periods through PBAC (Pictorial blood assessment charts) score.Timepoint: At the end of 2 months and 4 months after the start of treatment.
Secondary Outcome Measures
NameTimeMethod
1. Change in pain score after medication based on NRS (Numerical pain rating score). <br/ ><br>2. Patient satisfaction with treatment using TSQM (Treatment satisfaction questionnaire for medication).Timepoint: At the end of 2 months and 4 months after the start of treatment.
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