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Clinical Trials/IRCT20190227042862N1
IRCT20190227042862N1CompletedPhase 3

The effect of intraperitoneal instillation of Lidocaine on the postoperative pain after cesarean delivery

Mashhad University of Medical Sciences0 sites200 target enrollmentStarted: TBDLast updated:
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Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
200
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • •All pregnant women with singleton pregnancy
  • •between 18 to 45 years
  • •body mass index (BMI) less than 40
  • •one previous cesarean section with pfannenstiel incision
  • •candidate for elective cesarean section with spinal anesthesia

Exclusion Criteria

  • •history of other abdominal surgery
  • •history of chronic pain
  • •history of cardiac arrhythmia
  • •Sensitivity to the drugs which are used in the intervention group

Investigators

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