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Clinical Trials/CTRI/2018/05/014020
CTRI/2018/05/014020
Active, not recruiting
未知

Comparison of intravenous Paracetamol versus intravenous Tramadol for analgesia in labour

BPS Government medical college0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Pregnant women in active stage of labour
Sponsor
BPS Government medical college
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
BPS Government medical college

Eligibility Criteria

Inclusion Criteria

  • 1\. Primigravid and multigravid women of age ranges from 18 to 35 years with low risk to both mother and fetus (single live fetus in cephalic presentation without any associated obstetric and medical complication)
  • 2\. Women with gestational age ranges from 37 to 42 weeks
  • 3\. Women in active stage of labour (with cervical dilatation of 3\-5 cm and with moderate intensity uterine contractions of 2\-3 per 10 minutes each lasting for 30\-45 seconds with good inter relaxation period in between), whether spontaneous or induced labour
  • 4\. Women with reactive Non Stress Test (NST) before recruitment into study
  • 5\. Women seeking labour analgesia

Exclusion Criteria

  • 1\. Women with high risk pregnancy like severe Intrauterine growth retardation (IUGR), multiple gestation, malpresentation, polyhydroamnios, oligohydroamnios, pre\-mature rupture of membranes
  • 2\. Women with any medical disorder with pregnancy like severe anaemia, hypertensive disorders, diabetes mellitus, hypothyroidism
  • 3\. Women with scarred uterus
  • 4\. Women with obstetric indication for Lower Segment Caesarean Section before recruitment to study
  • 5\. Women in advanced stage of labour if cervical dilatation more than 5 cm
  • 6\. Women with use of any other kind of analgesia before recruitment to study
  • 7\. Women with previous history of hypersensitivity to Tramadol or Paracetamol
  • 8\. Women with deranged liver function test
  • 9\. Women not willing to participate in study

Outcomes

Primary Outcomes

Not specified

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