FindTrial
Sign In

A clinical study to compare the efficacy of sallakyadi oil vaginal tampon with powder of pushyanuga and balaguduchyadi oil vaginal tampon with powder of pushyanuga orally in the management of reproductive organ infection

An open label double arm randomised clinical study to compare the efficacy of sallakyadi taila yoni pichu with pushyanuga churna and balaguduchyadi taila yoni pichu with pushyanuga churna orally in the management of paripluta yonivyapat - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091555
Enrollment
40
Registered
2025-07-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: N739- Female pelvic inflammatory disease, unspecified

Interventions

None listed

Sponsors

Dr Shweta V Dattawadkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with symptoms mentioned in diagnostic criteria Patients presenting with the history of PID Mild to moderate PID

Exclusion criteria

Exclusion criteria: Pregnant women with Paripluta Severe and Acute Pelvic Inflammatory Disease and history of infections like Tuberculosis and HIV Paripluta in subjects having history of benign and malignant conditions of reproductive system

Design outcomes

Primary

MeasureTime frame
To evaluate and compare the efficacy of Sallakyadi Taila Yoni Pichu and Balaguduchyadi Taila Yoni Pichu with Pushyanuga Churna orally in the resolution of symptoms of Paripluta YonivyapatTimepoint: One and half year—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactDr Papiya Jana

sri kalabyraveshwara swamy ayurvedic medical college and research centre

drpapiya@gmail.com9886716216

Outcome results

None listed

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