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NCT00578136 · ClinicalTrials.gov registry record · NA
Analgesic Efficacy After Umbilical Hernia Repair in Children
A NA study, sponsored by Children's Hospital of Philadelphia.
- Completed
- Registry status
- NA
- Development phase
- 52
- Enrollment target
NCT00578136: Completed NA study, sponsored by Children's Hospital of Philadelphia.
NCT00578136 is a NA study that has completed, run by Children's Hospital of Philadelphia. The registered enrollment target is 52 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
NCT00578136, a NA study, has completed, sponsored by Children's Hospital of Philadelphia.
- COMPLETED
- Registry status
- NA
- Development phase
- 52 participants
- Enrollment target
Study Summary
Umbilical hernia repair is a common painful outpatient procedure performed in children. Often analgesia for this procedure is provided by using local infiltration of the surgical site by the surgeons and perioperative opioids and NSAIDS both IV and orally. The use of opioids can cause adverse side effects which include, but are not limited to nausea, vomiting, itching, and respiratory depression, etc. The rectus sheath block can be performed in these patients to decrease their post operative pain.
Primary Outcome
total postoperative opioid and any additional analgesic medications.
Interventions
- DRUG Bupivacaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2006-11 |
| Est. Completion | 2011-12 |
| Phase | NA |
What the finished NCT00578136 record still lists
NCT00578136 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 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 1 intervention - of which Bupivacaine is the first listed.
NCT00578136 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00578136 about?
NCT00578136 is a clinical study titled "Analgesic Efficacy After Umbilical Hernia Repair in Children". Umbilical hernia repair is a common painful outpatient procedure performed in children. Often analgesia for this procedure is provided by using local infiltration of the surgical site by the surgeons and perioperative opioids and NSAIDS both IV and orally. The use of opioids can cause adverse side e...
What is the current status of trial NCT00578136?
This trial is currently completed. It is a NA study. The enrollment target is 52 participants. The study started on 2006-11. Estimated completion is 2011-12.
What interventions are being tested in trial NCT00578136?
The interventions under investigation include: Bupivacaine (DRUG).
Who is sponsoring clinical trial NCT00578136?
This trial is sponsored by Children's Hospital of Philadelphia, which has 431 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00578136's enrollment target sits among peer trials
52 1272nd of 2000 higher than 722 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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