Clinical Trials Directory

Trials / Completed

CompletedNCT02440399

To Compare the Efficacy and Patients' Satisfaction for the Treatment of Post Cesarean Pain of Two Protocols: Oral Medications in Fixed Time Interval Administration Versus Spinal Morphine

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
200 (actual)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not 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.

Detailed description

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. Oral pain relievers' administration in fix protocol without need for patient demand 2. Spinal morphine given during the spinal anesthesia in the cesarean section

Conditions

Interventions

TypeNameDescription
DRUGTramadol hydrochloridePlease see arm description
DRUGMorphinePlease see arm description
DRUGParacetamol
DRUGDiclofenac
DRUGTAB. Percocet (Oxycodone 5MG/Paracetamol 325 MG)

Timeline

Start date
2015-07-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2015-05-12
Last updated
2017-05-09

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT02440399. Inclusion in this directory is not an endorsement.