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Neonatal Spinal Anesthesia: Effects of the Addition of Clonidine

NCT01075490 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2010-02-25

No results posted yet for this study

Summary

This prospective, double blinded study investigates spinal anesthesia with or without clonidine added to bupivacaine in newborns. This study is based on duration measurement of spinal anesthesia and cardio respiratory recording during 24h for apnea detection.

Conditions

  • Spinal Anesthesia
  • Neonates

Interventions

DRUG

clonidine

addition of 1 µg/kg of clonidine to bupivacaine 1 mg/kg as spinal anesthesia

DRUG

clonidine

equivalent volume of saline added to bupivacaine, 1 mg/kg as spinal anesthesia

Sponsors & Collaborators

  • University Hospital, Montpellier

    lead OTHER

Principal Investigators

  • Xavier Capdevila, PhD · CHU de Montpellier, France

  • Alain Rochette, MD · CHU de Montpellier, France

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Max Age
60 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2006-11-30
Completion
2009-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01075490 on ClinicalTrials.gov