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Effect of Unani drug on pain during menstruation

Comparative study of Abhal and Mefenamic Acid in Primary Dysmenorrhoea - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/039988
Enrollment
60
Registered
2022-02-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N944- Primary dysmenorrhea

Interventions

Intervention1: Abhal (J.communis L.): Orally 1.5g will be given thrice a day from day 1 to day 3 of menstruation for 2 consecutive months Control Intervention1: Mefenamic acid: 250 mg capsule of mefen

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women aged from 18 to 35 years with a history of regular menstrual cycle (28 ±7 days) with primary dysmenorrhoea .6 Having experienced menstrual pain of intensity from moderate to severe and the Visual Analog Scale >¬4cm for at least three menstrual cycles before this study.6 Primary dysmenorrhoea with or without associated symptoms like headache, dizziness, fever, nausea, vomiting, diarrhoea and fatigue.

Exclusion criteria

Exclusion criteria: Patient with secondary dysmenorrhoea, heavy menstrual bleeding and irregular menstrual cycles. Patient with malignancies. Patient taking OCPs6 and using intrauterine devices. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Change in VAS Scale for pain intensityTimepoint: Once every month during treatment for three months

Secondary

MeasureTime frame
Change in Health-related quality life assesses by SF12 Questionnaire and Change in uterine artery blood flow parameters (PI, RI and S/D ratio)Timepoint: At third month

Countries

India

Contacts

Public ContactArshiya Sultana

National Institute of Unani Medicine

drtaseen5nium@gmail.com7299129213

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026