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To understand the effect of erandmool arka in udavartini yonivyapad

Randomised controlled clinical control study to evaluate the efficacy of erandmool arka in udavarta yonivyapad with special refference to primary dysmenorrhoea - nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093370
Enrollment
60
Registered
2025-08-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

None listed

Sponsors

Dr. Dhanashri Devendra Shrikhande
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: clinically diagnosed cases of udavarta yonivyapad will be taken for study patient coming with chief complaints of painful menses suffering for at least 3 consecutive menstrual cycles patients with regular menstrual cycles and adequate menstrual flow not associated with any organic reproductive system abnormalities patients ready to participate in study with proper consent

Exclusion criteria

Exclusion criteria: patient having secondary dysmenorrhea patient age below 15 year and above 30 year anc and pnc patient patient on harmonal therapy or using an IUCD patient having any uterine or pelvic pathology patient with history of hypo/hyperthyroidism DM cardiovascular diseases

Design outcomes

Primary

MeasureTime frame
reduce pain before menses and during mensesTimepoint: reduce pain before menses and reduce symptoms of udavartini yonivyapd

Secondary

MeasureTime frame
no recurrence of symptoms of udavartini yonivyapadTimepoint: 21 days

Countries

India

Contacts

Public ContactDr Sunil Sadashiv More

Shree Sapatashrhungi Ayurved Mahavidyalay

moresunil263@gmail.com9423934505

Outcome results

None listed

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