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Clinical Trials/CTRI/2022/08/044572
CTRI/2022/08/044572
Not yet recruiting
未知

Comparison between intrathecal buprenorphine versus dexmedetomidine with hyperbaric Ropivacaine 0.75% in patients undergoing caesarean section.

ESIC Medical College Gulbarga0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: Z00-Z99- Factors influencing health status and contact with health servicesHealth Condition 2: O295- Other complications of spinal andepidural anesthesia during pregnancy

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: Z00-Z99- Factors influencing health status and contact with health servicesHealth Condition 2: O295- Other complications of spinal andepidural anesthesia during pregnancy
Sponsor
ESIC Medical College Gulbarga
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
ESIC Medical College Gulbarga

Eligibility Criteria

Inclusion Criteria

  • •Parturients with
  • •1\.Singleton pregnancy, scheduled for elective caesarean section under spinal anaesthesia
  • •2\.More than 36 weeks of gestation age
  • •3\.18\-40 years of age
  • •4\.Height between 140cm and 180cm
  • •5\.BMI less than 32kg/m2,
  • •6\.Nil per oral for more than 6 hours

Exclusion Criteria

  • •1\.Multiple pregnancy
  • •2\.Morbid Obesity (BMI \>40\)
  • •3\.Height \<140 cms \& \>170cms
  • •4\.Patients with spinal deformities and those who have undergone previous spine surgeries.
  • •5\.Pregnancy related hypertensive disease, preeclampsia, eclampsia.
  • •6\.Cardiovascular disease
  • •7\.Gestational diabetes requiring insulin.
  • •8\.Emergency caesarean sections for maternal or foetal distress.
  • •9\.Contraindication to spinal anesthesia.

Outcomes

Primary Outcomes

Not specified

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