NCT02004899View on ClinicalTrials.gov

Trial of Onset of Epidural Pain Relief With Low Dose Bupivacaine and Different Doses of Fentanyl in Laboring Women

PHASE3CompletedINTERVENTIONAL
Enrollment

105

Participants

Timeline

Start Date

December 31, 2013

Primary Completion Date

October 31, 2014

Study Completion Date

May 31, 2015

Conditions
Anesthetic, Sedative or Analgesic Complications in Labor or Delivery
Interventions
DRUG

Fentanyl

After obtaining informed consent, patients are randomized into one of two treatment groups or a control group by a computer generated random number table. After confirmation of epidural placement following test dose administration, a loading dose of 10 ml 0.08% Bupivacaine containing 20 mcg Fentanyl is administered after adding 1.6 ml 0.9% NaCl (Sodium Chloride) in the control group (F20).

Trial Locations (1)

N6A5W9

Victoria Hospital, London

All Listed Sponsors
collaborator

University of Western Ontario, Canada

OTHER

lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

NCT02004899 - Trial of Onset of Epidural Pain Relief With Low Dose Bupivacaine and Different Doses of Fentanyl in Laboring Women | Biotech Hunter | Biotech Hunter