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Clinical Trials/CTRI/2022/04/041914
CTRI/2022/04/041914
Not yet recruiting
Phase 2

A comparative study of labour analgesia between epidural analgesia and combined spinal epidural analgesia using bupivacaine and fentanyl in primiparous parturients.

Rajendra Institute of Medical Sciences Ranchi0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: O80- Encounter for full-term uncomplicated delivery

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Sponsor
Rajendra Institute of Medical Sciences Ranchi
Status
Not yet 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
Rajendra Institute of Medical Sciences Ranchi

Eligibility Criteria

Inclusion Criteria

  • •1\. Only booked primigravida parturient with all antenatal investigations within normal limits.
  • •2\. ASA physical status I and II.
  • •3\. Age group between 18\-35 years.
  • •4\. Height \> 140 cms.
  • •5\. Patients with full term singleton pregnancy (gestational age between 37\-42 weeks) in active phase of first stage of labour with good uterine contractions and cervical dilatation 3\-5 cm with vertex presentation.
  • •6\. Cervical dilation \>3 cm and \<5 cm.

Exclusion Criteria

  • •1\. ASA grade III and IV.
  • •2\. Age \<18 years or \>35 years.
  • •3\. Preterm gestation.
  • •4\. Patients who did not give consent.
  • •5\. Patient with severe anaemia, bleeding disorders, coagulation abnormalities or on anticoagulant therapy or history of prolonged aspirin ingestion.
  • •6\. Patients with spine deformity.
  • •7\. Patients with history of spine surgery.
  • •8\. Patient with history of chronic backache.
  • •9\. Patients with pre\-existing neurological or spinal disease, cardiovascular or respiratory impairment, local or systemic infection, cephalopelvic disproportion, feto placental insufficiency.
  • •10\. Fetal distress.

Outcomes

Primary Outcomes

Not specified

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