Last updated: April 11, 2024
Sponsor: Egymedicalpedia
Overall Status: Active - Recruiting
Phase
N/A
Condition
Uterine Disorders
Heavy Bleeding / Heavy Periods
Dysfunctional Uterine Bleeding
Treatment
Mefenamic acid 500 mg
Clinical Study ID
NCT06369012
Rania Gamal
Ages 15-45 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Any female patient in Child bearing period aging from 15-45 years complaining ofAbnormal uterine.
- Abnormal uterine bleeding due to endometrial, uterine cavity lesions as diagnosed byTVS or bleeding tendency e.g. Thrombocytopenia, Platelets dysfunction and coagulationdefects
Exclusion
Exclusion Criteria:
- Personal history of renal or hepatic impairment; previous thromboembolic disease,peptic ulcer.
- Females with evident drugs intake that cause AUB e.g warfarin, low molecular weightheparin.
- Vaginal, vulvar, and cervical causes of bleeding.
- Bleeding on top of Use of hormonal and non-hormonal contraception.
Study Design
Total Participants: 130
Treatment Group(s): 1
Primary Treatment: Mefenamic acid 500 mg
Phase:
Study Start date:
March 01, 2024
Estimated Completion Date:
September 30, 2024
Study Description
Connect with a study center
Ain Shams University Hospitals
Cairo,
EgyptActive - Recruiting
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