跳至主要内容
临床试验/CTRI/2025/03/082285
CTRI/2025/03/082285尚未招募2 期

An open randomized controlled clinical study to evaluate the efficacy of ushir churna with godugdha in stanyakshaya.

Dr Kalyani Harishchandra Sapkal1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
To evaluate the efficacy of Ushir Churna with Godugdha in Stanyakshay

研究概览

简要总结

This is randomised open controlled clinical study to evaluate the efficacy of Ushir Churna with Godugdha in stanyakshay observation will be made upon symptoms of Stanyakshay in sutika .Study will be carried out in OPD and IPD of stree roga prasuti tantra department of Yashwant ayurvedic rugnalaya, kodoli.

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
21.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • IN MOTHER 1)Patients willingly participating in the trial and giving informed written consent form.
  • Age group of patients between 21 to 35 years 3)Patients having sign and symptoms of stanyakshaya .
  • Patients from third day of Post partum (both LSCS and FTND) 5) Patients irrespective of primigravida or multigravida were selected.
  • IN BABY 1) Full term normal weight (2.5 to 3.5kg) mother side baby.

排除标准

  • IN MOTHER 1)Cracked or flat nipples.
  • Mastitis 3) History of breast trauma and surgery.
  • Patient under epileptic and Psychotic drugs.
  • IN BABY 1)Low birth weight baby(not allowing breast milk).

结局指标

主要结局

To evaluate the efficacy of Ushir Churna with Godugdha in Stanyakshay

时间窗: On 7th day, 15th day , 30th day

次要结局

  • 1)To increase Breastmilk secretion.(2)To assess stanza vruddhi by subjective parameter.)

研究者

发起方
Dr Kalyani Harishchandra Sapkal
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Kalyani Harishchandra Sapkal

Yashwant Ayurvedic College Postgraduate training and Research centre Kodoli, District Kolhapur

研究点 (1)

Loading locations...

相似试验