Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.

Status:

UNKNOWN

Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.

Lead Sponsor:

Soroka University Medical Center

Conditions:

Pain

Cesarean Delivery

Eligibility:

FEMALE

18-45 years

Phase:

Brief Summary

The objective of this prospective, double-blinded, placebo-controlled, randomized study is to evaluate the impact of preemptive analgesia using incisional site infiltration of lidocaine as compared to...

Detailed Description

The studied population would be based on women who are scheduled for an elective cesarean delivery under general/spinal analgesia using a transverse lower abdominal incision. Prior to each operation,...

Eligibility Criteria

Inclusion

Women who are scheduled for an elective cesarean delivery under general/spinal analgesia using a transverse lower abdominal incision.

Exclusion

More than two previous cesarean deliveries
Other abdominal operations in the past
Morbid obesity
Diabetes mellitus, neurological diseases, systemic vascular disease.
Mental disability
Lidocaine sensitivity

Key Trial Info

Start Date :

Trial Type :

INTERVENTIONAL

End Date :

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT00737542

Last Update

November 26 2009

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