Clinical Trials Directory

Trials / Completed

CompletedNCT01764048

To Compare the Efficacy and Patient's Satisfaction From Pain Management of Women After Cesarean Section by Pain Relievers' Administration in Fix Protocol Compared to Protocol Following Demand

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
214 (actual)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

Cesarean deliveries are prevalent. Unlike other operations, quick recovery is required for the mother to nurture the newborn child and establishing an appropriate mother-child bonding. Therefore, effective pain management is crucial. In this study we would like to compare between two pain relievers' administration protocols: (1) pain relievers' administration in fix protocol (type of medications, dose and intervals) or (2) pain relievers' administration following demand (the same type and doses, however, medications will be given only following patient's request). The primary outcome will be patient satisfaction, pain control and the necessity of additional medications (rescue doses). The protocols will be used for the first 48 hours following surgery.

Conditions

Interventions

TypeNameDescription
DRUGFix protocolPlease see arm description
DRUGmedications following demand protocolPlease see arm description

Timeline

Start date
2012-11-01
Primary completion
2014-01-01
Completion
2014-06-01
First posted
2013-01-09
Last updated
2016-01-08

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01764048. Inclusion in this directory is not an endorsement.