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临床试验/CTRI/2023/09/057683
CTRI/2023/09/057683尚未招募4 期

Comparative Study Of Safety And Efficacy Of Intravenous Paracetamol Versus Intramuscular Tramadol As Labour Analgesic

SIKKIM MANIPAL INSTITUTE OF MEDICAL SCIENCES1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2023年9月23日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
104
试验地点
1
主要终点
To check the efficacy of intravenous paracetamol with intramuscular tramadol when used as labor analgesics

研究概览

简要总结

All women in early/active labor after admission will be explained about the study and the type of drugs being used. Consenting pregnant women will be divided into two groups by alternate methods.  When the enrolled woman goes into active phase of labor with cervical dilatation â‰¥ 4cm,with cervical effacement of 60% ,she will be administered Visual Analogue Scale for pain scoring, then she will be given either one of the following study drugs:

• 100 ml of 1 gram inj paracetamol single dose given over 10 minutes

•100mg of inj tramadol hydrochloride single dose IM given over 15 mins.

•Visual Analogue scale (VAS) will be used to assess pain intensity and will be recorded in register.

•Pain in both groups will be analyzed at 10 mins, 30 mins and then hourly after drug administration. If  VAS >6 at any time, additional analgesic will be added .

Labor will be monitored using a WHO modified partograph and termination of pregnancy will be as per standard. Fetal monitoring will be done using a electronic fetal monitor.

Mothers will monitored for 24 hours after delivery for any side-effects and Neonatal conditions will be assessed by the use of APGAR scoring system and the need for admission into the NICU

研究设计

研究类型
Interventional
分配方式
Other
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • Consenting women in early/active phase of labour at ≥37weeks gestation Singleton pregnancy with cephalic presentation.

排除标准

  • Multiple Pregnancy and mal-presentation Intrauterine fetal death Women who do not consent for the study.
  • <37 weeks period of gestation History of allergy to any of the study drugs.

结局指标

主要结局

To check the efficacy of intravenous paracetamol with intramuscular tramadol when used as labor analgesics

时间窗: 10 mins | 30mins | 1 hourly after the administration of drug

次要结局

  • To check the safety of injection paracetamol with injection tramadol when used as labor analgesics(0hrs to 24 hrs after delivery)

研究者

发起方
SIKKIM MANIPAL INSTITUTE OF MEDICAL SCIENCES
申办方类型
Private medical college

研究点 (1)

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