Clinical Trials Directory

Trials / Completed

CompletedNCT02115087

Efficacy Study of Rectus Sheath Block to Control Postoperative Pain

The Effect of Ultrasound Guided Rectus Sheath Block on Postoperative Analgesia After Laparotomy With Transverse Incision in Children

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Cukurova University · Academic / Other
Sex
All
Age
3 Years – 15 Years
Healthy volunteers
Not accepted

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.

Detailed description

Prospective, randomized study.Forty patients with American Society of Anaesthesiologists (ASA) I-II physical status, aged 3-15 years.Patients are randomly allocated into two groups and are administered general anesthesia and before the beginning of surgery ultrasound guided RSB with 0.2 ml.kg-1, 0.25% of levobupivacaine and thirty minutes before the surgery the loading dose of morphine of 0.1 mg.kg-1 intravenously are received in group RSB and group M, respectively. Patient controlled analgesia (PCA) device with 0.01 mg.kg-1 bolus dose of morphine and 30 minutes lockout interval is set up postoperatively in both groups.

Conditions

Interventions

TypeNameDescription
PROCEDUREultrasound guided rectus sheath blockthe application of rectus sheath block with ultrasound guidance
DRUGMorphine

Timeline

Start date
2010-09-01
Primary completion
2011-01-01
Completion
2011-01-01
First posted
2014-04-15
Last updated
2014-04-15

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02115087. Inclusion in this directory is not an endorsement.