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临床试验/CTRI/2025/02/081354
CTRI/2025/02/081354尚未招募2/3 期

A Randomized Controlled Clinical Study to evaluate add on effect of Shunthi Ghritha with Navayasa Loha in Panduroga vis-a-vis Iron Deficiency Anemia.

Dr Vajreshwari1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年3月20日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Reduction in symptoms of Panduroga assessed by subjective criteria

研究概览

简要总结

This study is a randomized, comparative clinical trail to evaluate the add on effect of Shunthi ghritha 12 grams twice daily along with Navayasa loha 500 mg twice daily in Group A with minimum of 15 patients, Navayasa loha 500 mg twice daily in Group B with minimum of 15 patients in the management of Panduroga vis-a-vis Iron deficiency anemia for a period  of 30 days. The primary outcome is reduction in symptoms of Panduroga and the secondary outcome is improvement in subjects condition.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

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

入选标准

  • Subjects of both gender between the age group of 20-60 years who fit into diagnostic criteria will be included.
  • Subjects presenting with pratyatma lakshana of Panduroga that include panduta, agnimandya, dourbalya, shrama, arohanaayasa, gatrashula, aruchi, bhrama, pindikodwestana, karnaksweda .etc.
  • Subjects with mild to moderate anemia with Hb concentration of 8-11.99% in females and 8-12.99% in males.
  • Subjects who are willing to provide informed consent will be included.

排除标准

  • Subjects having severe anemia with Hb less than 8gm% will be excluded from the study.
  • Subjects having any other systemic diseases and under medications which interfere with the disease process and the present clinical trial will be excluded.
  • Pregnancy, lactation and puerperal stage will be excluded.
  • Subjects suffering from bleeding disorders, infective, metabolic or endocrinal disorders and autoimmune diseases will be excluded.
  • Subjects known case of Sickle cell anemia, Thalassemia, Leukemia, Hemophilia, Sideroblastic anemia, etc.
  • will be excluded.

结局指标

主要结局

Reduction in symptoms of Panduroga assessed by subjective criteria

时间窗: 30th day

次要结局

  • Improvement in subjects condition assessed by objective criteria(30th day)

研究者

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

Dr Vajreshwari

Sushrutha Ayurvedic Medical College and Hospital

研究点 (1)

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