Intrathecal Opioid Study

Status Completed

Clinical Trial 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.

Clinical Trial Description

1. To evaluate the effect of three different intrathecal opioid mixtures on post-operative pain experiences in women who have undergone caesarean section surgery, relating specifically to:

1. Post-operative analgesic requirements at two time points (12 hours and 24 hours) after surgery

2. Pain scores at two time points (12 hours and 24 hours) after surgery

3. Sedation scores at two time points (12 hours and 24 hours) after surgery

4. Post-operative nausea scores at two time points (12 hours and 24 hours) after surgery

5. Post-operative pruritis scores at two time points (12 hours and 24 hours) after surgery

2. To determine the impact that the patients' post-operative pain has on their activities in the first 24 hours after surgery ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02577809
Study type	Interventional
Source	University of Witwatersrand, South Africa
Contact
Status	Completed
Phase	Phase 4
Start date	July 2015
Completion date	September 2015

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