Clinical Trials Directory

Trials / Completed

CompletedNCT02274974

Post-Caesarean Section Incisional Infiltration With Lidocaine Versus Lidocaine and Epinephrine

Post-Caesarean Section Incisional Infiltration With Lidocaine Versus Lidocaine and Epinephrine;Randomized Controlled Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Ain Shams Maternity Hospital · Academic / Other
Sex
Female
Age
18 Years – 38 Years
Healthy volunteers
Accepted

Summary

Study to compare between efficacy of post-caesarean section infiltration with lidocaine and epinephrine versus lidocaine only to reduce post-incisional pain.

Detailed description

assessment of adding of epinephrine to lidocaine as local infiltrator to post-caesarean section wound in prolongation of its anaesthetic effect.

Conditions

Interventions

TypeNameDescription
DRUGLidocaine•The wound of C.Swill be infiltrated before closure of the skin, with 20 ml of 2% lidocaine.
DRUGlidocaine and EpinephrineThe wound of C.S will be infiltrated before closure of the skin, with 20 ml of 2% lidocaine and epinephrine in related dose manner 1:200.000.

Timeline

Start date
2014-08-01
Primary completion
2015-03-01
Completion
2015-04-01
First posted
2014-10-27
Last updated
2015-06-25

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02274974. Inclusion in this directory is not an endorsement.

Post-Caesarean Section Incisional Infiltration With Lidocaine Versus Lidocaine and Epinephrine (NCT02274974) · Clinical Trials Directory