Status:
COMPLETED
Post-Caesarean Section Incisional Infiltration With Lidocaine Versus Lidocaine and Epinephrine
Lead Sponsor:
Ain Shams Maternity Hospital
Conditions:
Pain, Postoperative
Eligibility:
FEMALE
18-38 years
Phase:
PHASE4
Brief 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.
Eligibility Criteria
Inclusion
- Women undergoing caesarean delivery under General anesthesia for various indications.
- Women refuse spinal anesthesia.
Exclusion
- Known or suspected sensitivity to local anesthesia.
- Medical disorders induced by pregnancy (Pre-eclamptic toxemia, gestational diabetes mellitus, Hepatic diseases, homeostatic disorder)
- Medical disorders aggravated by pregnancy (cardiovascular disease, pulmonary disease, renal disease, neurological disease, metabolic or infectious diseases).
- Women who hemo-dynamically unstable.
- Lack of adequate verbal communication.
Key Trial Info
Start Date :
August 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2015
Estimated Enrollment :
160 Patients enrolled
Trial Details
Trial ID
NCT02274974
Start Date
August 1 2014
End Date
April 1 2015
Last Update
June 25 2015
Active Locations (1)
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1
Post-Caesarean Section Incisional Infiltration With Lidocaine Versus Lidocaine and Epinephrine;
Cairo, Egypt, 11511