跳至主要内容
临床试验/CTRI/2017/05/008524
CTRI/2017/05/008524招募中2/3 期

A Controlled Comparative clinical Study of Efficacy of Bala Taila in the Management of Episiotomy Wound

Parul Institute of Ayurved1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年6月16日最近更新:

试验速览

阶段
2/3 期
状态
招募中
发起方
入组人数
40
试验地点
1
主要终点
Change in Standardized REEDA Scale (Redness, Edema, Ecchymosed, Discharge and Approximation) and Numerical Rating Scale (NRS) (‘0-10’ point pain intensity scale)

研究概览

简要总结

Episiotomy is common procedure in obstetric practice. Incidence is 56% in india. There is scope to control pain and woundhealingthrough ayurvedic medicine. Drug use in this study has properties like  wound healing, antiinflammatory and analgesic. By using standard scales assessment done.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
20.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • 1 Primipara patients who undergo vaginal delivery with episiotomy will be selected.
  • 2 Patient between ages 20 to 35 will be selected.
  • 3 No history of disease impaired wound healing.
  • 4 Those patient who ready to sign the inform consent form will be included only.

排除标准

  • 1 Multipara.
  • 2 Patients with 3rd and 4th degree perineal tear or injury to rectum / urethra 3 Patients with any other major illnesses e.g. HIV, HbSAg, VDRL positive,cancer.
  • 4 Patients with history of delayed wound healing, IDDM, gestational diabetes, congenital bleeding disorders.

结局指标

主要结局

Change in Standardized REEDA Scale (Redness, Edema, Ecchymosed, Discharge and Approximation) and Numerical Rating Scale (NRS) (‘0-10’ point pain intensity scale)

时间窗: within 10 days outcome assessed

次要结局

  • Change in Standardized REEDA Scale (Redness, Edema, Ecchymosed, Discharge and Approximation) and Numerical Rating Scale (NRS) (‘0-10’ point pain intensity scale)(within 10 days outcome assessed)

研究者

发起方
Parul Institute of Ayurved
申办方类型
Private medical college

研究点 (1)

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