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NCT01740193 · ClinicalTrials.gov registry record · NA
Comparison of Two Different Pain Management Techniques in Pediatric Patients Undergoing a Hernia Repair
A NA study, sponsored by Children's Hospital Medical Center, Cincinnati.
- Completed
- Registry status
- NA
- Development phase
- 59
- Enrollment target
NCT01740193: Completed NA study, sponsored by Children's Hospital Medical Center, Cincinnati.
NCT01740193 is a NA study that has completed, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 59 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
NCT01740193, a NA study, has completed, sponsored by Children's Hospital Medical Center, Cincinnati.
- COMPLETED
- Registry status
- NA
- Development phase
- 59 participants
- Enrollment target
Study Summary
The purpose of this research study is to find the best way to decrease pain in children right after surgery whom have had their hernia fixed. Right now, there are two different ways surgeons and anesthesia providers try to decrease pain. It is not clear if one way is better than the other. The method used is often chosen by which one the doctor has more experience using. The Investigator plans to find out if one of the methods is more effective and/or safer than the other method. The results of this study will help learn how to best control pain in children having surgery for hernia repair.
Primary Outcome
Worst FLACC score observed in the post-anesthesia care unit by the research coordinator during the first post-operative hour
Interventions
- PROCEDURE TAP Block
- PROCEDURE Ilioinguinal/iliohypogastric blockade
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 59 participants |
| Start Date | 2012-08 |
| Est. Completion | 2017-12 |
| Phase | NA |
What the finished NCT01740193 record still lists
NCT01740193 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 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 TAP Block is the first listed.
NCT01740193 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01740193 about?
NCT01740193 is a clinical study titled "Comparison of Two Different Pain Management Techniques in Pediatric Patients Undergoing a Hernia Repair". The purpose of this research study is to find the best way to decrease pain in children right after surgery whom have had their hernia fixed. Right now, there are two different ways surgeons and anesthesia providers try to decrease pain. It is not clear if one way is better than the other. The metho...
What is the current status of trial NCT01740193?
This trial is currently completed. It is a NA study. The enrollment target is 59 participants. The study started on 2012-08. Estimated completion is 2017-12.
What interventions are being tested in trial NCT01740193?
The interventions under investigation include: TAP Block (PROCEDURE), Ilioinguinal/iliohypogastric blockade (PROCEDURE).
Who is sponsoring clinical trial NCT01740193?
This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01740193's enrollment target sits among peer trials
59 1256th of 2000 higher than 745 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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