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Mayaphal Taila Yoni Pichu &Udumbara Taila Yoni Pichu in Yonishaithilya (Perineal Laxity)

Comparative study of Mayaphal Taila Yoni Pichu &Udumbara Taila Yoni Pichu in Yonishaithilya (Perineal Laxity)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030310
Enrollment
50
Registered
2021-01-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: MAYAPHALTAILA: YONI PICHU DOSE 10 ML Intervention2: Mayaphal Taila: Mayaphal Taila Yoni Pichu Route of administration-Intravaginally Dose-10ML Frequency- once (at night) Total duratio

Sponsors

Department of Prasuti Tantra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Married women of age group 25-45 yrs with regular menses who complain of something coming out per vagina,Patients of different gravidity and parity,Patients complaining of heaviness in external genitalia, vaginal discharge, micturition disturbances, coital difficulties with any associated symptom,Patient willing to participate in study.

Exclusion criteria

Exclusion criteria: Pregnant women,Psychologically unstable patient ,Patients with metabolic disorders like any systemic disease, thyroid dysfunction, hypertension,Patients with 3rd degree uterine prolapse,Patients with pelvic inflammatory diseases,Patients suffering from any genital tract infection or under treatment of STDS, HIV, HBSAg et,Patients having congenital abnormalities in genital tract,Patient having any benign & malignant growth of genital tract, polyp, fibroid,Patients with any history of allergy or allergy from trial drug,Congenital elongation of cervix,Patient with any surgical history of genital tract,Patients with decubitous ulcer with 3rd degree uterine prolapse.

Design outcomes

Primary

MeasureTime frame
Assessment will be done on basis of prepared proforma and improvment in sign and symptoms of yonishaithilyaTimepoint: Total 5 follow ups will be done at every 15 days. Four (4) follow ups will be done with medication and 5th follow up will be done without medication to see the changes in parameters.

Secondary

MeasureTime frame
Improvement in criteria listed in different scalesTimepoint: Total 5 follow ups will be done at every 15 days. Four (4) follow ups will be done with medication and 5th follow up will be done without medication to see the changes in parameters.

Countries

India

Contacts

Public ContactDr Pournima Gadge

Banaras Hindu University

ssom18@gmail.com7607165096

Outcome results

None listed

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