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Clinical Trials/CTRI/2022/06/043450
CTRI/2022/06/043450
Not yet recruiting
Phase 2

Comparative study of low dose intrathecal Midazolam and Fentanyl as an adjuvant to Bupivacaine heavy in patients undergoing elective caeserian section under spinal anaesthesia -A Prospective Randomized Double Blind Clinical Study.

Government Medical College Vadodara0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Sponsor
Government Medical College Vadodara
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
Government Medical College Vadodara

Eligibility Criteria

Inclusion Criteria

  • •1\.Patients undergoing Elective caesarean section under spinal anesthesia.
  • •2\.Age 18\-40yrs.
  • •3,ASA I andII.
  • •4\.Height \-150 cm and above

Exclusion Criteria

  • •1\.Patients refuse spinal anesthesia; unwilling to participate in study,unable to communicate.
  • •2\. Patients with localized skin infection, haemorrhagic diathesis ,neurological involvement/ gross spinal abnormality,severe anemia.
  • •3\.Patients with history of drug allergy to Bupivacaine, fentanyl and midazolam.
  • •4\.Patients with cardiac, pulmonary,hepatic or renal disorders.
  • •5 Bad obstetric history, obstetric complications in present pregnancy, evidence of foetal compromise and anomalies.
  • •6 Patients physically dependent on narcotics or benzodiazepines.
  • •7\.Patients unable to understand Visual analog scale.

Outcomes

Primary Outcomes

Not specified

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