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临床试验/CTRI/2026/03/106822
CTRI/2026/03/106822尚未招募1 期

Comparative clinical study to evaluate the efficacy of Udumbaradi Taila with Guduchidantyadi Malhar in the management of Acharana Yonivyapad with special reference to Pruritus Vulvae.

Chandra Shekhar Singh Ayurved Chikitsalaya evam Shodh Kedra1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年4月6日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Relief in Yoni Kandu (itching)

研究概览

简要总结

Acharana Yonivyapad is a gynecological disorder described in Ayurveda, mainly caused due to improper genital hygiene, leading to symptoms like itching (kandu) in the vulval region. It is clinically correlated with Pruritus Vulvae, which is commonly associated with vaginal discharge, burning sensation, dyspareunia and discomfort. Conventional treatments such as antibiotics and antifungals may cause side effects and disturb normal vaginal flora.

The present study is a randomized comparative clinical trial to evaluate the efficacy of Udumbaradi Taila Yoni Pichu and Guduchidantyadi Malhar in the management of Acharana Yonivyapad. A total of 60 patients will be randomly divided into two groups. Group A will receive Udumbaradi Taila Yoni Pichu and Group B will receive Guduchidantyadi Malhar for local application, for 7 days after cessation of menstruation for 3 consecutive cycles.

The outcome will be assessed based on improvement in symptoms like itching, vaginal discharge, malodour, pain, dyspareunia and vaginal pH. This study aims to evaluate a safe, effective and cost-efficient Ayurvedic management for Pruritus Vulvae.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • Adult female who are in age group of 18-45 years.
  • Only married patient.
  • Patients having pruritus vulvae as a cardinal symptom with or without vaginal discharge.

排除标准

  • Patients below 18yrs and above 45yrs.
  • Patient unwilling to participate in trial.
  • Patients after menopause.
  • Patient of uterine prolapse &Carcinoma.
  • Patient on oral contraceptives, or using intrauterine contraceptive devices.
  • Patients with diabetes mellitus, tuberculosis, jaundice, severe HTN.
  • Patients with extensive chronic cervicitis, fibroid and malignancy.
  • VDRL, HIV, HBsAg ,HCV positive patient.

结局指标

主要结局

Relief in Yoni Kandu (itching)

时间窗: 3 months

次要结局

  • Yoni srava(Daurgandhya)

研究者

发起方
Chandra Shekhar Singh Ayurved Chikitsalaya evam Shodh Kedra
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Akanksha Shukla

Chandra Shekhar Singh Ayurvedic Sansthan

研究点 (1)

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