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To evaluate the efficacy of Udumbarashalatu Siddha taila yonipichu in upapluta yonivyapad

Efficacy Of Udumbarashalatu Siddha Taila Yonipichu In The Management Of Upapluta Yonivyapad -An Open Label Double Arm Randomized Controlled Clinical Study - nill

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109534
Enrollment
40
Registered
2026-04-28
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: O235- Infections of the genital tract inpregnancy

Interventions

None listed

Sponsors

Dr Shinde Rutuja Mohan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with the upapluta yonivyapad. 2.Patient aged 21 years and above irrespective of parity. 3. After completion of first trimester of pregnancy.

Exclusion criteria

Exclusion criteria: l. Women suffering from any systemic disease like Diabetes Mellitus, T.B, H.I.V 2.Patients with cervical encirclage and lesions interfering with treatment.

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of Udumbarashalatu siddha Taila yonipichu in the signs and symptoms of Upapluta Yonivyapad.Timepoint: Assessment will be done before treatment ,Day 7, After 7 days of treatment

Secondary

MeasureTime frame
To compare the effect of Udumbarashalatu siddha Taila & Dhatakyadi taila Yonipichu in the management of upapluta yonivyapad.Timepoint: Assessment will be done before treatment ,Day 7, After 7 days of treatment

Countries

India

Contacts

Public ContactDr Shinde Rutuja Mohan

SHRI DHARAMASTHALA MANJUNATHESHWARA INSTITUTE OF AYURVEDA AND HOSPITAL

dr.pramodinip@gmail.com8496841492

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026