Study to evaluate the Efficacy of Phalaghrita orally and as yonipichu in the management of Pittaj Yonivyapad

Randomized controlled clinical trial to evaluate the efficacy of Phalaghrita orally and in the form of yonipichu in the management of Pittaj Yonivyapad - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/05/109910

Enrollment

Registered

2026-05-04

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Health Condition 1: N72- Inflammatory disease of cervix uteri

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient having sign of Pittaj yonivyapad. 2)Married patients. 3)Non pregnant patients. 4)Patients willing to give consent for this study. 5)Patients willing for regular follow up

Exclusion criteria

Exclusion criteria: 1)Unmarried patients 2)Patients with venereal disease, diabetes. 3)Patients with IUCD. 4)Antenatal and postnatal patients. 5)Suspected case of CA cervix. 6)Patients with Uterine prolapse. 7)Diagnosed cases of STDs.

Design outcomes

Primary

Measure	Time frame
Yonidaha reduces,post coital bleeding reduces,yonipaka reduces,yonigat strava reduces, vrana ropanaTimepoint: 14 days	—

Secondary

Measure	Time frame
To compare the efficiency of Phalaghrit orally and as yonipichu with Yashtimadhu siddha tail yonipichu in the management of Pittaj yonivyapad. To study Pittaj yonivyapad as per Ayurvedic view. To study cervical erosion according to modern viewTimepoint: 14 days	—

Countries

India

Contacts

Public ContactDr Sayli Rajesh Bhargav

CSMSS Ayurved Mahavidyalaya and Rugnalaya,Kanchanwadi Aurangabad

dr.jayashrisdeshmukh@gmail.com9325580777

Outcome results