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Effect of Unani drugs with Mefenemic Acid in painful menstruatio

Not Applicable
Completed
Conditions
Health Condition 1: null- DysmenorrheaHealth Condition 2: N944- Primary dysmenorrhea
Registration Number
CTRI/2017/10/010168
Lead Sponsor
ational Institute of Unani Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
64
Inclusion Criteria

1. Patients aged from 14 to 35 years with a history of regular menstrual cycle (28±7 days) with spasmodic dysmenorrhea.

2. Having experienced menstrual pain of intensity from moderate to severe and the Visual Analog Scale > 4 cm for at least three menstrual cycles before this study.

Exclusion Criteria

1. Patients with secondary dysmenorrhea, and irregular menstrual cycles.

2. Patients using OCPs and contraceptive devices.

3. Patients with systemic diseases and malignancies.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome was decrease of more than 50% of pain severity on Visual Analogue Scale (VAS) score for pain intensity. <br/ ><br>Pain relief was assessed by pain relief scaleTimepoint: third and fifth month
Secondary Outcome Measures
NameTimeMethod
Secondary outcome:â?¢Health related quality of life assessed by SF 12 and safety assessment <br/ ><br>Timepoint: Visit 3
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