dsyapereunia female sexual dysfunction

An open clinical trial to evaluate the effect of Yonipichu with Dhanvantara taila in Paripluta Yonivyapat wsr to Dyspareunia

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/12/010947

Enrollment

Registered

2017-12-21

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: null- FEMALE COMPLAINING OF PAIN DURING THE SEXUAL INTERCOURSE

Interventions

Intervention1: DHANVANTARA TAILA: DHANVANTARA TAILA IN YONI PICHU FORM 30ml 7 days daily once Control Intervention1: none: none

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pain during the intercourse 2. Dry vagina 3. Failure of orgasm 4. Married female patients of sexually active group 20- 45yrs

Exclusion criteria

Exclusion criteria: 1. Tough imperforate hymen 2. Narrow introitus 3. Pregnancy 4. Known cases of Benign and malignant condition of cervix 5. Known cases of Veneral diseases

Design outcomes

Primary

Measure	Time frame
1.Reduction in pain during intercourse according to VAS scale 2.Increase in number of sexual intercourse weeklyTimepoint: 1.Reduction in pain during intercourse according to VAS scale 2.Increase in number of sexual intercourse weekly	—

Secondary

Measure	Time frame
noneTimepoint: none	—

Countries

India

Contacts

Public ContactDrNamrataBBhagaje

KLEUS SHRI BMK AYURVEDIC MAHAVIDYALAYA PG AND RESEARCH CENTRE SHAHPUR BELAGAVI

bnamratabhagaje@gmail.com7204727997

Outcome results

None listed

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