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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 is a NA study that has completed, run by Boston Children's Hospital. The registered enrollment target is 53 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01015053
The ClinicalTrials.gov registry entry for NCT01015053 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 53 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Children's Hospital, which has 462 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which bilateral ultrasound-guided rectus sheath block is the first listed.
NCT01015053 reports 0 study locations.
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.
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