CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 40 enrolled
Drug / intervention
Continuous infusion of ropivacain in ESP catheter +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03593642
NCT03593642N/ACompleted
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Bilateral Erector Spinae Plane (ESP) Catheters Versus Single Shot ESP Block for Open Heart Surgery in Infants

Vinmec Healthcare System·interventional·Posted Jul 20, 2018·Updated Feb 24, 2020

In Brief

A clinical study evaluating Continuous infusion of ropivacain in ESP catheter and Continuous infusion of Iso Saline in ESP catheter for Opioid Use and 2 related conditions. Completed, enrolled 40 participants across 1 site.

Detailed Summary

Post operative pain after open heart surgery is still a main concern; current multimodal analgesia modalities have shown good efficacy for postoperative pain at rest, without reaching full pain relief. The primary goal of this study is to evaluate the effectiveness of peri-operative analgesia, measured by consumption of opioids during the first 48h hours after the surgery, using bilateral erector spinae catheters for 48h, compared to single shot erector spinae block in pediatric patients undergoing open heart surgeries .

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOpioid Use, Pain, Postoperative, Quality of Life
CountriesVietnam
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedJul 20, 2018
Enrollment StartOct 1, 2018
Primary CompletionApr 1, 2019
Study CompletionJun 30, 2019
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 8.0 years ago

Interventions

Continuous infusion of ropivacain in ESP catheterdrug

administration of ropivacaine in ESP catheter to provide regional analgesia after surgery

Continuous infusion of Iso Saline in ESP catheterdrug

administration of Iso Saline in ESP catheter to be the control group