Clinical Trials Directory

Trials / Unknown

UnknownNCT04618146

Enhanced Recovery After Cesarean Section With Low Dose Intrathecal Morphine.

Enhanced Recovery After Cesarean Section With Low Dose Intrathecal Morphine. A Prospective Randomized Controlled Study.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Minia University · Academic / Other
Sex
Female
Age
16 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study is designed to see the effect of low dose intrathecal morphine on promting enhanced recovery after cesarean delivery with early ambulation and reduction of hospital stay.

Detailed description

Parturients showing for elective cesarean section will be randomized into 3 groups by a computer generated randomization list. Each randomization slip will be put in a sealed envelope until patient enrollment. Patients will be divided into Group C: control group, given intrathecal bupivacaine 12.5 mg. Group M25: intrathecal bupivacaine 12.5mg + morphine 25 microgram. Group M50: intrathecal bupivacaine 12.5mg + morphine 50 microgram.

Conditions

Interventions

TypeNameDescription
DRUGMorphine Sulfateintrathecal low dose morphine for early return to normal activity without opioid related complications.
DRUGBupivacaine Hydrochlorideintrathecal bupivacaine 0.5%

Timeline

Start date
2020-11-10
Primary completion
2021-03-01
Completion
2021-03-01
First posted
2020-11-05
Last updated
2021-03-01

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04618146. Inclusion in this directory is not an endorsement.