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Efficacy Study of Rectus Sheath Block to Control Postoperative Pain

NCT02115087 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-04-15

No results posted yet for this study

Summary

The aim of this study is to evaluate the effect of the ultrasound guided rectus sheath block (RSB) on both intraoperative sevoflurane consumption and postoperative analgesia.

Conditions

  • Pain, Postoperative

Interventions

PROCEDURE

ultrasound guided rectus sheath block

the application of rectus sheath block with ultrasound guidance

DRUG

Morphine

Sponsors & Collaborators

  • Cukurova University

    lead OTHER

Principal Investigators

  • Dilek Ozcengiz, Prof. · Department of Anesthesiology, Cukurova University Faculty of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
3 Years
Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2011-01-31
Completion
2011-01-31

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT02115087 on ClinicalTrials.gov