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Intrathecal Opioid Study

NCT02577809 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-10-16

No results posted yet for this study

Summary

This is an interventional drug trail to evaluate the effect of different intrathecal opioids on post-operative pain experiences in women who have undergone caesarean section surgery.

Conditions

  • Post-operative Pain

Interventions

DRUG

Morphine100

100mcg added to the spinal anaesthetic

DRUG

Morphine50

50mcg added to the spinal anaesthetic

DRUG

Fentanyl

25mcg Fentanyl added to the spinal anaesthetic

DRUG

Hyperbaric Bupivicaine

1.8ml 0.5% spinal bupivicaine with dextrose

DRUG

Indomethacin

100mg Indomethacin suppository

Sponsors & Collaborators

  • University of Witwatersrand, South Africa

    lead OTHER

Principal Investigators

  • Sean Chetty, FCA(SA) · University of Witwatersrand, South Africa

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2015-09-30
Completion
2015-09-30

Countries

  • South Africa

Study Locations

More Related Trials

Entities

Drugs

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 NCT02577809 on ClinicalTrials.gov