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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: Completed NA study, sponsored by Seattle Children's Hospital.
NCT00836134 is a NA study that has completed, run by Seattle Children's Hospital. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
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 |
What the finished NCT00836134 record still lists
NCT00836134 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 2 interventions - of which rectus sheath block is the first listed.
NCT00836134 does not publish any study locations in the registry export this page uses.
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
How this trial's enrollment target compares
Where NCT00836134's enrollment target sits among peer trials
40 1447th of 2000 higher than 465 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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