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To Evaluate the Effect of Panchavalkaladi TailaYoni Pichu Dharan in the Management of Acharana Yonivyapad

Randomised Controlled Clinical Trial to Evaluate the Effect of Panchavalkaladi TailaYoni Pichu Dharan in the Management of Acharana Yonivyapad with Special Reference to Pruritus Vulvae - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080728
Enrollment
76
Registered
2025-02-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system

Interventions

None listed

Sponsors

Dr Sayali Bharatkumar Vengurlekar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Female having per vaginal itiching. 2) Age between 18-70 yrs married female patient. 3) Female who are willing to participate

Exclusion criteria

Exclusion criteria: ) Pregnant women 2) Local gynaecological causes like ovarian cyst, prolapse, fibromyoma, polyps. 3) Neoplasm (Cervical or uterine malignancy) 4) patients with bleeding disorders 5) Those suffering from congenital anomalies of genital tract 6) Pelvic inflammatory diseases 7) Patients with sexually transmitted diseases 8) Abnormal uterine bleeding 9) Patients with severe hepatic or cardiac or renal disorders 10) Those having leukaemia or platelet deficiency disorders 11) Females in their puerperium period 12) Patient with severe anaemia 13) HIV HbsAg VDRL,HPV positive patients 14) Patients with DM,HTN

Design outcomes

Primary

MeasureTime frame
Significantly reduction in PruritusTimepoint: 8 days

Secondary

MeasureTime frame
Significantly reduction in Pruritus by using Panchavalkayadi tail yoni pichu than Nimb tail yoni pichuTimepoint: 8 days

Countries

India

Contacts

Public ContactDrManoj Vitthal Gaikwad

R.A.Podar Medical Ayu College Worli

drmanojvgaikwad@gmail.com9822752816

Outcome results

None listed

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