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study of unani formulation in painful periods

Phase 2
Conditions
Health Condition 1: null- Dysmenorrhoea
Registration Number
CTRI/2018/03/012646
Lead Sponsor
ational Institue of Unani Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients with age group of 18-35 years.

Patients with regular menstrual cycle and painful menstruation

Exclusion Criteria

Patients with,

Intra uterine contraceptive devices.

Organic pelvic pathology.

Systemic illness.

Allergic /sensitive to NSAIDs.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
changes in subjective parameters.Timepoint: During treatment before and after menstrual cycle. <br/ ><br>After treatment once in a month for one cycle. <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
â?¢Painful menstruation associated with nausea /vomiting /diarrhoea /giddiness/ and headache.Timepoint: During treatment before and after menstrual cycle. <br/ ><br>After treatment once in a month for one cycle. <br/ ><br>
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