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NCT01015053 · ClinicalTrials.gov registry record · NA
Postoperative Pain After Pediatric Umbilical Hernia Repair
A NA study, sponsored by Boston Children's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 53
- Enrollment target
NCT01015053: Completed NA study, sponsored by Boston Children's Hospital.
NCT01015053 is a NA study that has completed, run by Boston Children's Hospital. The registered enrollment target is 53 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01015053, a NA study, has completed, sponsored by Boston Children's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 53 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the use of ultrasound-guided bilateral rectus sheath blocks to local infiltration of anesthetic agent in the surgical wound in a pediatric population of patients undergoing umbilical hernia repair.
Interventions
- PROCEDURE bilateral ultrasound-guided rectus sheath block
- PROCEDURE Wound infiltration
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 53 participants |
| Start Date | 2009-11 |
| Est. Completion | 2011-11 |
| Phase | NA |
What the finished NCT01015053 record still lists
NCT01015053 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 53 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which bilateral ultrasound-guided rectus sheath block is the first listed.
NCT01015053 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01015053 about?
NCT01015053 is a clinical study titled "Postoperative Pain After Pediatric Umbilical Hernia Repair". The purpose of this study is to compare the use of ultrasound-guided bilateral rectus sheath blocks to local infiltration of anesthetic agent in the surgical wound in a pediatric population of patients undergoing umbilical hernia repair.
What is the current status of trial NCT01015053?
This trial is currently completed. It is a NA study. The enrollment target is 53 participants. The study started on 2009-11. Estimated completion is 2011-11.
What interventions are being tested in trial NCT01015053?
The interventions under investigation include: bilateral ultrasound-guided rectus sheath block (PROCEDURE), Wound infiltration (PROCEDURE).
Who is sponsoring clinical trial NCT01015053?
This trial is sponsored by Boston Children's Hospital, which has 462 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01015053's enrollment target sits among peer trials
53 1271st of 2000 higher than 729 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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