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Study to evaluate Ayurvedic treatment (Chaturbeeja Churna and Matra Basti with Effect of Chaturbeeja Churna and Matra Basti with Saindhavadi Taila in primary dysmenorrhea (painful periods)

Clinical evaluation of the efficacy of Chaturbeeja Churna and Matra Basti with Saindhavadi Taila in the management of Kashtartava with special reference to Primary Dysmenorrhea - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107945
Enrollment
60
Registered
2026-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Chandra Shekhar Singh Ayurved Chikitsalaya evam Shodh Kendra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with history of painful menstruation for at least three consecutive cycles. Individuals willing to participate in the study and give written consent (parental consent for minors below 18 years)

Exclusion criteria

Exclusion criteria: Patient with Irregular menstruation cycle, Menorrhagia & Metrorrhagia. Patient with gynaecological disorders such as fibroids, ovarian cyst, endometriosis, or malignancy. Patient with severe systemic illness (like uncontrolled Diabetes, Hypertension or Thyroid Disorder). Patient with IUCD. Patient unwilling or unable to comply with treatment protocol

Design outcomes

Primary

MeasureTime frame
Assessment of reduction in pain during menstruation (Kashtartava) before and after treatmentTimepoint: 3 Months—

Secondary

MeasureTime frame
Assessment of associated symptoms such as lower abdominal pain duration, backache, nausea, vomiting, and effect on daily activities before and after treatmentTimepoint: 90 Days—

Countries

India

Contacts

Public ContactProf Dr Mayank Kesharwanee

Chandra Shekhar Singh Ayurvedic Sansthan

swarnima0914@gmail.com7355930914

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026