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A clinical trail of Ayurvedic therapy in management of painful menses

A randomised controlled trial to evaluate the efficacy of Hinguwadi gutika and Rajahpravartini vati in the Management of Udavarta Yonivyapad W.S.R. to Primary Dysmenorrhea.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044092
Enrollment
30
Registered
2022-07-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

NATIONAL INSTITUTE OF AYURVEDA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. PATIENTS WITH CHIEF COMPLAINT OF PAIN DURING MENSES ALONG WITH ASSOCIATED SYMPTOMS. 2. PATIENTS WHO HAVE MENSTRUAL PAIN SCORE MORE THAN GRADE I ACCORDING TO VERBAL MULTIDIMENSIONAL SCORING SYSTEM (VMSS). 3. PATIENTS WHO HAD REGULAR MENSTRAL CYCLES OF 23-35 DAYS IN THE LAST 3 MONTHS. 4. PATIENT IN AGE GROUP OF 18 TO 30 YEARS 5. PATIENTS WITH H/O USING ANALGESICS DURING MENSES. 6. PATIENT WILLING TO GIVE VOLUNTARY INFORMED CONSENT FOR THE STUDY.

Exclusion criteria

Exclusion criteria: The patient suffering from any severe systemic, or autoimmune disorders, specially those who are mentioned as Asadhya vyadhi as per clinical text of Ayurveda will be excluded. Subjects having organic pathology of uterus and adnexa like Fibroid uterus,carcinoma of endometrium, endometriosis etc. 1 having pelvic inflammatory disease or 2 chronic leucorrhoea. 3 Patients who vaccinated for covid19 with in past three month.

Design outcomes

Primary

MeasureTime frame
1. NRS â?? Scale: Numeric Rating Scale for DysmenorrhoeaTimepoint: 60 DAYS

Secondary

MeasureTime frame
1. VMSS scale: Verbal Multidimensional Scoring SystemTimepoint: 60 DAYS

Countries

India

Contacts

Public ContactPROF DR K BHARATHI

NATIONAL INSTITUTE OF AYURVEDA

baruhunt@gmail.com9492047131

Outcome results

None listed

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