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临床试验/CTRI/2025/09/095099
CTRI/2025/09/095099尚未招募4 期

A Comparative study of 0 point 1 percent Ropivacaine with or without Fentanyl for Epidural Labour analgesia A Randomized Controlled study

RNT Medical College1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年10月6日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
80
试验地点
1
主要终点
To compare the VAS score in both groups

研究概览

简要总结

The goal of our present study is a comparative study of 0.1% Ropivacaine alone or with  Fentanyl (2 mcg/ml) for Epidural Labour Analgesia in randomized controlled double blind study with regard to VAS score ( pain intensity score), duration of different stages of labour, time of onset of analgesia,hemodynamic parameters,Neonatal assessment (APGAR Score), patient satisfaction score ,Complications related to drug/epidural catheter.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

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

入选标准

  • Age between 18 and 35 years
  • ASA grade I and II in active stage of labour (greater than or equal to 3 cm dilatation)
  • Primigravida
  • Singleton pregnancy
  • Vertex presentation
  • Uncomplicated pregnancy
  • Parturients requesting labour analgesia.

排除标准

  • Patient refusal
  • ASA grade III and IV
  • Age greater than 35 years and less than 18 years
  • Multipara patients(greater than 2 children)
  • Comorbid conditions like Severe cardiac disease, Severe Pregnancy induced Hypertension, Eclampsia, Severe anemia, Psycological/Neurological disease
  • Complicated preganancies like Cephalo Pelvic disproportion, Breech presentation, Cord around neck and Previous Caesarean section.
  • Local sepsis
  • Altered coagulation profile
  • Bleeding disorders, thrombocytopenia
  • Spinal deformities
  • History of allergy to study drug.

结局指标

主要结局

To compare the VAS score in both groups

时间窗: 0,5,15,30,45,60,90 minutes,every hourly maximum up to 8hrs

次要结局

  • Time of onset of analgesia,Total dose of analgesia required,Total duration of labour,Neonatal outcome,Patient satisfaction score(0,5,15,30,45,60,90 min,every hourly maximum up to 8hrs, APGAR Score at 1 & 5 min.)

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Devendra Verma

RNT Medical College & MB Hospital,Udaipur.

研究点 (1)

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