Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00836134 · ClinicalTrials.gov registry record · NA
Ultrasound-guided Rectus Sheath Block for Post-operative Pain Control Following Umbilical Hernia Repair
A NA study, sponsored by Seattle Children's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
NCT00836134 is a NA study that has completed, run by Seattle Children's Hospital. The registered enrollment target is 40 participants.
The verdict
NCT00836134, a NA study, has completed, sponsored by Seattle Children's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the effectiveness of local infiltration to an ultrasound guided nerve block placed by the anesthesiologist for children undergoing umbilical hernia repair. This is a double-cohort, double blinded, randomized study comparing local infiltration to ultrasound-guided rectus sheath block in children 1 to 17 years of age undergoing epigastric or umbilical hernia repair. We will first compare pain scores to see if one method is more adequate then the other in providing post-op analgesia. Our second aim is to compare morphine consumption between the two groups. Our third aim is to measure the levels of local anesthetic in the blood following local anesthetic infiltration or USGRSB.
Interventions
- PROCEDURE rectus sheath block
- PROCEDURE local anesthetic infiltration
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2009-02 |
| Est. Completion | 2010-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00836134
The ClinicalTrials.gov registry entry for NCT00836134 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seattle Children's Hospital, which has 168 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which rectus sheath block is the first listed.
NCT00836134 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00836134 about?
NCT00836134 is a clinical study titled "Ultrasound-guided Rectus Sheath Block for Post-operative Pain Control Following Umbilical Hernia Repair". The purpose of this study is to compare the effectiveness of local infiltration to an ultrasound guided nerve block placed by the anesthesiologist for children undergoing umbilical hernia repair. This is a double-cohort, double blinded, randomized study comparing local infiltration to ultrasound-gu...
What is the current status of trial NCT00836134?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2009-02. Estimated completion is 2010-06.
What interventions are being tested in trial NCT00836134?
The interventions under investigation include: rectus sheath block (PROCEDURE), local anesthetic infiltration (PROCEDURE).
Who is sponsoring clinical trial NCT00836134?
This trial is sponsored by Seattle Children's Hospital, which has 168 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.