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Clinical Trials/CTRI/2022/08/044691
CTRI/2022/08/044691
Not yet recruiting
Phase 4

Randomised double blinded prospective study to compare the effects of 0.75% Ropivacaine heavy and 0.5% Bupivacaine heavy in subarachnoid block for caesarean delivery in obstetric patients

Mytily0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: O80- Encounter for full-term uncomplicated delivery

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Sponsor
Mytily
Status
Not yet recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Mytily

Eligibility Criteria

Inclusion Criteria

  • •Obstetric patients coming for elective caesarean section
  • •Age group of 20\-40 years
  • •ASA 1 \& ASA 2 patients
  • •Full term pregnant patients
  • •Patients with Single live intrauterine fetus

Exclusion Criteria

  • •1\.Patients who refuse
  • •2\.Emergency surgeries
  • •3\.Age group \<20 or \>40 years of age
  • •4\.ASA 3 \& ASA 4 patients
  • •5\.Pre term patients
  • •6\.Multiple pregnancy (twin or more gestation)
  • •7\.Associated comorbid conditions( PIH, GDM, Anaemia, Heart disease)
  • •8\.Bleeding diathesis patients
  • •9\.Fetal indication for caesarean delivery

Outcomes

Primary Outcomes

Not specified

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