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临床试验/CTRI/2024/09/073194
CTRI/2024/09/073194尚未招募3 期

Efficacy of pre-defined Homoeopathic medicines in mother tincture vis - a - vis 30c potency in the management of renal calculi - parallel arm comparative clinical study

Dr. Khyati Lakhani1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年9月14日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
Renal pain Episode

研究概览

简要总结

This study is a parallel arm comparative clinical study to evaluate and compare the efficacy of Predefined Homoeopathic medicines (Berberis Vulgaris, Hydrangea Arborescens, Lycopodium Clavatum, Sarsaparilla, Uva Ursi) in mother tincture vis a vis 30C potency in the management of renal calculi. The primary outcome measures will be Renal pain episode assessed at every 2 weeks and renal stone size assessed at 0-6 months or as an when required by USG KUB. The secondary outcomes will be removal of renal stone which is assessed at 6 months after onset of treatment or till removal of stone, whichever is earlier by USG KUB.

研究设计

研究类型
Interventional

入排标准

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

入选标准

  • Age group 18 to 60 years.
  • Both genders.
  • Patients giving voluntary consent for the study.
  • Stone in region of kidney, ureter, bladder or in urethra.
  • Diagnosed cases of Renal calculi on basis of USG KUB reports.

排除标准

  • Pregnant and lactating females.
  • Staghorn renal calculi.
  • The patients having severe hydronephrosis.
  • The cases requiring emergency treatment.

结局指标

主要结局

Renal pain Episode

时间窗: Assessing Frequency every 2 weeks

次要结局

  • Renal stone size(• USG KUB from 0 to 6 months after onset of the treatment or as an when required,)
  • Removal of Renal stone(•6 months after onset of treatment or till removal of stone, whichever is earlier)

研究者

发起方
Dr. Khyati Lakhani
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Khyati Lakhani

Homoeopathy University

研究点 (1)

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