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To study the Efficacy Of Shallakyadi Taila Pichu In The Management Of Vipluta Yonivyapada with especial refference of pruritus vulvae

A Randomized Controlled Clinical Trial To Evaluate Efficacy Of Shallakyadi Taila Pichu And Nystatin Pessary In The Management Of Vipluta Yonivyapad With Special Reference Of Pruritus Vulvae - NA

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089904
Enrollment
60
Registered
2025-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: N899- Noninflammatory disorder of vagina, unspecified

Interventions

None listed

Sponsors

Vijaylaxmi Munshilal Maurya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient having sign and symptoms of vipluta yonivyapada having symtooms like yoni kandu,aatiratipriya, nitya yonivedana,such patient will be randomly selected from prasuti tantra stree roga opd of late kedari redekar ayurvedic hospital

Exclusion criteria

Exclusion criteria: unmarried,pregnant and lactational, H/O-DM, Patient associated with Genital TB infection,HIV,HBsAG,VDRL postive, Patient with benign and malignant tumor of buterus and cervix, patient who need surgical intervention in cases like pelvis abscess, Tubo-ovarian mass.

Design outcomes

Primary

MeasureTime frame
The primary outcome focuses on the clinical efficacy of Shallakyadi Taila Pichu versus Nystatin pessary in managing Vipluta Yonivyapad, with special reference to pruritus vulvae. It will be assessed based on symptomatic relief (Yonikandu, Yonistrava, Yonivedana, Dyspareunia, Dysuria). Assessment will occur at baseline, during treatment, post-treatment, and follow-ups.Timepoint: 15 days

Secondary

MeasureTime frame
NilTimepoint: NIL

Countries

India

Contacts

Public ContactDr Sarita Harshal Kamate

Late Kedari Redekar Ayurvedic Mahavidyalaya

saritakamate9@gmail.com9881988389

Outcome results

None listed

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