To evaluate the efficacy of guduchyadi yonivarti in Upaplutha yonivyapath, vulvovaginitis during pregnancy

An Open Label Double Arm Randomised Controlled Clinical Study On Efficacy Of Guduchyadi Yonivarti In Upaplutha Yonivyapath Vulvovaginitis During Pregnancy - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070215

Enrollment

Registered

2024-07-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: O235- Infections of the genital tract inpregnancy

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Primi and multi gravida 2.Second and third trimester 3.Subjects with lakshanas of upapluta yonivyapad – yoni srava , yonikandu 4.Subjects with age group of 20 to 40 years

Exclusion criteria

Exclusion criteria: 1.Subjects with age less than 20 years and more than 40 years 2.First trimester 3.Subjects suffering from systemic illness like Diabetes milletus , hypertension ,UTI 4.Subjects suffering from Sexually Transmitted Disease

Design outcomes

Primary

Measure	Time frame
Significant reduction in signs and symptoms of Upapluta yonivyapath, vulvovaginitis during pregnancy based on gradingTimepoint: Baseline, 15 days	—

Secondary

Measure	Time frame
Improved quality of life and prevent recurrence in patients diagnosed with Upapluta yonivyapath, vulvovaginitis during pregnancy based on gradingTimepoint: Baseline, 15 days	—

Countries

India

Contacts

Public ContactDr Ankitha M

Sri dharmasthala manjunatheshwara institute of ayurveda and hospital ,Bangalore

dranusham@sdmayurbangalore.in8105777424

Outcome results