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Clinical Trials/CTRI/2018/06/014589
CTRI/2018/06/014589
Recruiting
Phase 1

Efficacy and safety of intravenous paracetamol versus intramuscular tramadol hydrochloride as intrapartum analgesic: a randomised controlled study

government0 sites0 target enrollmentTBD
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Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
government
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

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
government

Eligibility Criteria

Inclusion Criteria

  • •1\. Primigravidae in spontaneous labour
  • •2\. Active phase of labour (cervical dilation of \>\=4cm,in the presence of adequate uterine 3 contractions per 10 minutes and each lasting at least for 40 seconds)
  • •3\. Maternal age between 18 to 35 years
  • •4\. Singleton term pregnancy(37 \- 42 weeks of gestation)
  • •5\. vertex\- presenting fetus

Exclusion Criteria

  • •1\. clinical evidence of cephalopelvic disproportion
  • •2\. Malpresentation
  • •3\. scrred uterus , previous cesarean section, hysterotomy or myomectomy
  • •4\.medical disorders associated with pregnancy, especially severe anemia, jaundice, hypertension,diabetes, renal impairment
  • •5\. Fetal distress
  • •6\. Receiving any regional or parenteral analgesia before recuitment in the study.
  • •7\. Known hypersensitoivity to the drug family
  • •8\. induced labour

Outcomes

Primary Outcomes

Not specified

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