At a glance
ClinicalIndex Comparison RecordN/ACompleted· 281 enrolled
Drug / intervention
Femoral nerve block with ropivacaine or bupivacaineprocedure
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.
A Retrospective Investigation of Safety and Efficacy From Increasing Concentrations of Local Anesthetic in Pediatric Femoral Nerve Blocks
In Brief
An observational study evaluating Femoral nerve block with ropivacaine or bupivacaine for Postoperative Pain. Completed, enrolled 281 participants.
Detailed Summary
The purpose of this study is to retrospectively compare perioperative pain relief and safety in pediatric patients who have received a femoral nerve block with varying concentrations of local anesthetic.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPostoperative Pain
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartJun 2015
First PostedJul 2015
Primary CompletionMay 2016
TodayJul 2026
First PostedJul 17, 2015
Enrollment StartJun 1, 2015
Primary CompletionMay 1, 2016
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 11.0 years ago
Interventions
Femoral nerve block with ropivacaine or bupivacaineprocedure