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临床试验/CTRI/2024/12/078155
CTRI/2024/12/078155已完成2/3 期

Clinical Comparative Study to Evaluate the Efficacy of Yashtyadi Kwath and Yashtyadi Kwath with Narikel Jal Anupan in the Management of Pittaj Mutrakruccha with Special Reference to Urinary Tract Infection

Shree Saptashrungi Ayurved MahavidyalayaKamal nagar Hiravadi Panchavati Nashik1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年12月24日最近更新:

试验速览

阶段
2/3 期
状态
已完成
发起方
入组人数
70
试验地点
1
主要终点
Reduce The Sign And Symptoms Of Pittaj Mutrakruccha

研究概览

简要总结

OBJECTIVES

Primary Objective:

  1. To compare the efficacy of Yashtyadi kwatha and Yashtyadi kwatha with anupan narikel jal in Pittaj Mutrakrucchra with special reference to urinary tract infection.

  2. To study the efficacy of Yashtyadi kwath in Pittaj Mutrakruchhra with special reference to Urinary tract infection.

Secondary Objective:

  1. To study the disease Pittaj Mutrakrucchra in Detail According to Ayurved.

  2. To Study urinary tract infection in Detail.

  3. Study the efficacy of Yashtyadi kwatha in Pittaj mutrakruchchra with special reference to UTI

  4. Study the efficacy of Yashtyadi kwath with anupan narikel jal in Pittaj Mutrakrucchra with special reference to urinary tract infection .

PARTICIPANTS

70 Adults diagnosed with urinary tract infection meeting inclusion and exclusion criteria from OPD and IPD of department of shalyatantra of Shree Saptashrungi Medical College and Hospital Nashik

Interventions

35 patients Yashtyadi Kwath : Administered according to standardized protocol.

35 patients Yashtyadi Kwath with Narikel Jal anupan : Administered according to standardized protocol.

Primary Outcome :

Reduce the sign and symptoms of pittaj mutrakruccha

Secondary Outcome:

No recurrency of pittaj mutrakruccha

Treatment Duration : 7 Days

Follow Up :0th , 7th , 14th Days

Data Analysis : Data will be analysed using appropriate statistical methods to compare the effectiveness of the intervension on the primary and secondary outcomes.

Ethical Considerations : The study will be conducted in accordence with ethical guidelines and with informed consent from participents.

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients having sign and symptoms of Pittaj Mutrakruchra (Sadaha, Sapeet, Saruja Mutrapravruti).
  • The age group between 18 to 60 years.
  • Patients irrespective of religion, sex and economical status.
  • Patients with urinary tract infection.
  • Patients having recurrent UTI.

排除标准

  • Pregnancy & lactation
  • Prostate enlargement
  • Patients who having Malignancy of any part of urinary tract.
  • Phimosis or paraphimosis
  • Patients who having Renal failure, chronic kidney diseases, Renal calculus.
  • Sever Traumatic causes
  • Patients who having DM, HTN, Asthma, HIV, HbsAg..
  • Bleeding during micturition due to renal calculus .
  • Patients who having autoimmune disorder.

结局指标

主要结局

Reduce The Sign And Symptoms Of Pittaj Mutrakruccha

时间窗: 7 Days

次要结局

  • No Reccurency Of Pittaj Mutrakruccha(14 Days)

研究者

发起方
Shree Saptashrungi Ayurved MahavidyalayaKamal nagar Hiravadi Panchavati Nashik
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Amol Ashok Bhuite

Shree Saptashrungi Ayurved Mahavidyalaya,Kamal nagar Hiravadi, Panchavati, Nashik,

研究点 (1)

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