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Effect of Chaturbeeja choorna in the management of primary dysmenorrhoea i.e., painful menstruation.

An open label single arm clinical study on the effect of Chaturbeeja choorna in the management of Udavartini Yonivyapath vis-à-vis Primary Dysmenorrhea. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062406
Enrollment
30
Registered
2024-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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 Anushree A B C
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with regular cycles complaining of painful menstruation for at least 3 consecutive cycles.

Exclusion criteria

Exclusion criteria: Pelvic pathology - known case of fibroid, adenomyosis, endometriosis, pelvic inflammatory disease, menorrhagia, malignancy. Patients with intrauterine contraceptive devices or on contraceptive pills Congenital anomalies of reproductive systems Metabolic disorders - known case of diabetes mellites, hypertension, thyroid dysfunction.

Design outcomes

Primary

MeasureTime frame
To know the effect of Chaturbeeja choorna in the management of Primary Dysmenorrhoea.Timepoint: 3 consecutive cycles follow up will be done on each cycle the assessment of any improvement in objective and subjective parameters will be assessed .

Secondary

MeasureTime frame
The effect of drug on over all development & improvement pertaining general condition & haemoglobin levels will be assessedTimepoint: 3 consecutive cycles follow up will be done on each cycle the assessment of any improvement in objective & subjective parameters will be assessed .

Countries

India

Contacts

Public ContactDr Nanda K O

JSS Ayurveda Medical College And Hospital

nandadeepak.dr@gmail.com8970322532

Outcome results

None listed

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