Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.

NCT00737542 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2009-11-26

No results posted yet for this study

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 saline solution on post operative pain control in women undergoing cesarean deliveries.

Conditions

  • Pain
  • Cesarean Delivery

Interventions

DRUG

lidocaine

DRUG

NACL 0.9%

Sponsors & Collaborators

  • Soroka University Medical Center

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • Israel

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00737542 on ClinicalTrials.gov