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NCT03834454

Bupivacaine 5 mg vs 7.5 mg for Spinal Anesthesia in Cesarean Delivery in Indonesian Population

Completed NA Last updated 11 February 2019
What this trial tests

NA trial testing Bupivacaine in Cesarean Section in 112 participants. Completed in 31 December 2013.

Timeline
1 October 2013
Primary endpoint
31 December 2013
31 December 2013

Quick facts

Lead sponsorIndonesia University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposesupportive care
Enrollment112
Start date1 October 2013
Primary completion31 December 2013
Estimated completion31 December 2013
Sites1 location across Indonesia

Drugs / interventions tested

Conditions studied

Sponsor

Indonesia University

Who can join

Adults 18 to 40, female only, with Cesarean Section or Hypotension Drug-Induced. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to evaluate the efficacy of hyperbaric 5 mg bupivacaine + fentanyl 25 mcg versus hyperbaric 7.5 mg bupivacaine + fentanyl 25 mcg to lower incidence of hypotension

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. How Low Can We Go? A Double-Blinded Randomized Controlled Trial to Compare Bupivacaine 5 mg and Bupivacaine 7.5 mg for Spinal Anesthesia in Cesarean Delivery in Indonesian Population.
    Chandra S, Nugroho AM, Agus H, Susilo AP. · · 2019 · cited 6× · PMID 31341830 · DOI 10.5812/aapm.91275

Verify or expand the search:

Other trials of Bupivacaine

Trials testing the same drug.

Other recruiting trials for Cesarean Section

Currently open trials in the same condition.

Other Indonesia University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03834454.

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