Skip to content

Herbal treatment for dysmenorrhea

Effect Of Zafran In Primary Dysmenorrhea- Pre & Post Interventional Study without control group

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/052139
Enrollment
30
Registered
2023-04-28
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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: Cap Zafran 250mg BD: cap zafran 250mg twice daily for 5 days. Control Intervention1: NIL: NIL

Sponsors

National institute of unani medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Painful menstrual cycles with or without associated symptoms(nausea, vomitting, fatigue)

Exclusion criteria

Exclusion criteria: Patients with systemic disease HTN, DM-II. Patients with pelvic pathologies(Fibroid, PID, Endometriosis, PCOS, Malignancies) Patients with acute abdominal conditions(Appendicitis, Renal colic) Patients on HRT previous three months. Lactating women.

Design outcomes

Primary

MeasureTime frame
Subjective: Painful menstruation mild to moderate as per VAS.Timepoint: 90 days

Secondary

MeasureTime frame
Objective: VAS & VMS, SF-12(Qol)Timepoint: 90 days

Countries

India

Contacts

Public ContactProf Wajeeha Begum

National Institute of Unani Medicine

drwajeehanium@gmail.com9972550185

Outcome results

None listed

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