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NCT02352519 · ClinicalTrials.gov registry record · Phase 4
A Comparison of UGBRS Block and Local Infiltration
A Phase 4 study, sponsored by Baylor College of Medicine.
- Completed
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
NCT02352519 is a Phase 4 study that has completed, run by Baylor College of Medicine. The registered enrollment target is 50 participants.
The verdict
NCT02352519, a Phase 4 study, has completed, sponsored by Baylor College of Medicine.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
Study Summary
In this research study, the investigators are trying to find out which of the two methods of injecting local anesthetics (at the site of the belly button cut or by ultrasound guided rectus sheath block) will provide better pain relief and less need for pain medication after surgery in children undergoing single incision laparoscopic appendectomy.
Interventions
- PROCEDURE UGBRSB
- PROCEDURE Local Infiltration
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2011-04 |
| Est. Completion | 2015-06 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02352519
The ClinicalTrials.gov registry entry for NCT02352519 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which UGBRSB is the first listed.
NCT02352519 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02352519 about?
NCT02352519 is a clinical study titled "A Comparison of UGBRS Block and Local Infiltration". In this research study, the investigators are trying to find out which of the two methods of injecting local anesthetics (at the site of the belly button cut or by ultrasound guided rectus sheath block) will provide better pain relief and less need for pain medication after surgery in children under...
What is the current status of trial NCT02352519?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2011-04. Estimated completion is 2015-06.
What interventions are being tested in trial NCT02352519?
The interventions under investigation include: UGBRSB (PROCEDURE), Local Infiltration (PROCEDURE).
Who is sponsoring clinical trial NCT02352519?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
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