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A Study Of Ayurveda And Modern Therapy In Heavy Menstrual Bleeding With Special Reference To Guna Siddhant

A Comparative study of Ayurveda and Modern Therapy in Asrigdara(Menorrhagia) with special reference to Guna Siddhant

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040475
Enrollment
60
Registered
2022-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified

Interventions

None listed

Sponsors

Department of Siddhant Darshan Faculty of Ayurveda Institute of Medical Sciences BHU
Lead Sponsor
Department of Prasuti Tantra Stri Roga and Department of Obstetrics and Gynecology
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Married women of age group 21 to 40 years. 2. Women having complaint of excessive menstrual bleeding from three cycles or more than three cycles. 3. Patients willing to participate in above mentioned trial and giving informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients associated with any currently ongoing research study. 2. Patients having history of recent delivery or abortion. 3. Patients using any hormonal preparation. 4. Patients with any specific disease specially of chronic nature such as marked anaemia, T.B., hypertension , diabetes , hypo/hyper thyroidism, cardiac disease, renal disease, jaundice or any other disorders influencing general physical health and ultimately influencing menses. 5. Patients having organic lesion of reproductive system such as cervical erosion, benign or malignant growth, extensive cervical carcinoma, cervical polyp, recto-vaginal fistula, uterovaginal prolapse, endometriosis, tubercular endometritis etc. 6. Psychiatric patients. 7. Patients having any allergy to the drugs.

Design outcomes

Primary

MeasureTime frame
Assessment will be done on the basis of prepared proforma for assessment of subjective parameter This completely depends upon the symptomatology & its gradesTimepoint: 4 months duration divided into 4 followups of 1 month

Secondary

MeasureTime frame
To evaluate the effect of Tranexa, To evaluate the effect of Shalmali Ghrit Uttar Basti,To evaluate the effect of Mocharasa ChurnaTimepoint: 4 months duration divided into 4 followups of 1 month

Countries

India

Contacts

Public ContactProf Rani Singh

Banaras Hindu University

bhuranisingh@gmail.com8601095944

Outcome results

None listed

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