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Ayurvedic management of pain during periods

A single blind randomized comparative clinical trial to evaluate the efficacy of Panchkola Arka and Chaturbeeja Arka in the management of Udavartini Yonivyapad (Primary Dysmenorrhea) - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079570
Enrollment
60
Registered
2025-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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 SHIVANI SHARDA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects fulfilling the diagnostic criteria Subjects of Age group 18 to 30 years Married and unmarried women Subjects with regular menstrual cycles with the interval of 24 to 38 days History of painful menstruation for atleast 3 consecutive cycles Subjects without any structural pelvic pathology

Exclusion criteria

Exclusion criteria: Subjects experiencing menstrual pain attributed to underlying pelvic pathology diagnosed by USG like uterine fibroids adenomyosis endometriosis etc Subjects with Intrauterine contraceptive devices IUCDs Subjects with uncontrolled diabetes hypothyroidism and hypertension Subjects with a history of undiagnosed irregular vaginal bleeding Subjects who habitually consume analgesics antispasmodics sedatives or muscle relaxants within 48 hours before expected menstrual periods Subjects on Progesterone or Estrogen Pills Subjects with any structural pelvic pathology

Design outcomes

Primary

MeasureTime frame
80 % reduction in scoring of WALIDD Timepoint: from 0th to 90th day

Secondary

MeasureTime frame
Reduction in associated symptomsTimepoint: from 0th to 90th day

Countries

India

Contacts

Public ContactDR HARPREET

Shri Dhanwantry Ayurvedic College And Hospital

harpreet.minni@gmail.com9417039027

Outcome results

None listed

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