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NCT03860402

The Effect of Warm Local Anesthetic Solution on Epidural Anesthesia

Completed Last updated 6 March 2020
What this trial tests

trial testing Temperature in Cesarean Section in 50 participants. Completed in 31 January 2020.

Timeline
1 February 2019
Primary endpoint
31 December 2019
31 January 2020

Quick facts

Lead sponsorHallym University Kangnam Sacred Heart Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment50
Start date1 February 2019
Primary completion31 December 2019
Estimated completion31 January 2020
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Hallym University Kangnam Sacred Heart Hospital

Who can join

Adults 20 to 45, female only, with Cesarean Section. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators are going to compare the onset and duration of nerve blockage with the use of pre-warmed (38°C) and room temperature (20°C) local anesthetic solutions (ropivacaine and fentanyl) on epidural anesthesia for cesarean section, and compare the incidence of complications such as hypotension, nausea and vomiting.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Temperature

Trials testing the same drug.

Other recruiting trials for Cesarean Section

Currently open trials in the same condition.

Other Hallym University Kangnam Sacred Heart Hospital trials

Trials by the same sponsor.

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Data sources for this page

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