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Efficacy of unani drug in painful menstruation

Efficacy of Hilteet in Usre Tams (Dysmenorrhoea): A Single-Blind Randomized Standard Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/02/006655
Enrollment
60
Registered
2016-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- patients with dysmenorrhea

Interventions

Intervention1: Oleo-gum-resin of Ferual assafoetida: 250 mg twice daily for 5 days
2 days prior the menses and first three days of menstruation Control Intervention1: Mefenamic acid: 250 mg twice daily for 5 days
2 days prior the menses and first three days of menstruation

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age >= 12 years (age between menarche and menopause). Patients complaining of dysmenorrhea symptoms and menstrual cramps persisting for the past six months. Patients with regular menstrual cycle ranging from 21 to 35 days, scanty or average bleeding during periods.

Exclusion criteria

Exclusion criteria: • Pain caused by inflammatory or malignant diseases 17 • Patients below 12 years • Patients with chronic general illness • Lactating women • Patients using OCP. • Patients having problem of menorrhagia10

Design outcomes

Primary

MeasureTime frame
Main outcome: Change in Visual analogue scale score for pain intensity Timepoint: change in visual analogue scale score for pain intensity will be assessed at BL and after treatment

Secondary

MeasureTime frame
Secondary outcome : Change in quality of life assessed by SF-36 Questionnaire Timepoint: two months treatment and one month follow up

Countries

India

Contacts

Public ContactArshiya Sultana

National Institute of Unani Medicine

drarshiya@yahoo.com09740915911

Outcome results

None listed

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