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Asarun versus Sumbul ul teeb in Premenstrual symptoms associated with menstraution

Efficacy of Asarun versus Sumbul ul teeb in Premenstrual Syndrome- A randomised clinical study

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081003
Enrollment
64
Registered
2025-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: N943- Premenstrual tension syndrome

Interventions

Intervention1: Asarun: Asarun 3 gm daily orally in 2 divided doses from 15 day prior to the expected menstrual cycle for 3 consequent cycles Control Intervention1: Sumbul-ut-teeb: Sumbul-ut-teeb 4 gm

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18 and 35 years. Having a regular menstrual cycle with a cycle length of 21-35 days. Presenting with symptoms of premenstrual syndrome (diagnosed by ACOG criteria). Having a minimum PMTS score more than 17 and VAS score more than 4.

Exclusion criteria

Exclusion criteria: Patients with any organic pelvic pathology,Use of hormonal therapy or oral contraceptives in past 3 months,A known systemic or metabolic disease (Thyroid disease, Diabetes mellitus, Hypertension).

Design outcomes

Primary

MeasureTime frame
Reduction in PMTS ScoreTimepoint: Follow up will be done monthly for 3 consecutive cycles during the trial and once after the completion of trial.

Secondary

MeasureTime frame
Reduction in VAS ScoreTimepoint: Follow up will be done monthly for 3 consecutive cycles during the trial and once after the completion of trial

Countries

India

Contacts

Public ContactDr Kouser Fathima Firdous

National Institute of Unani Medicine

kouser2fathima@gmail.com9743730208

Outcome results

None listed

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