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NCT01500655 · ClinicalTrials.gov registry record · NA
Ultrasound-Guided Block of the Lateral Femoral Cutaneous Nerve in Pediatric Patients
A NA study of Burns, sponsored by Massachusetts General Hospital.
- Completed
- Registry status
- NA
- Development phase
- 19
- Enrollment target
- 1
- Study location
NCT01500655 is a NA study of Burns that has completed, run by Massachusetts General Hospital. The registered enrollment target is 19 participants, below the 83-participant average among 36 other Burns trials with a reported enrollment target (77% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01500655, a NA study of Burns, has completed, sponsored by Massachusetts General Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 19 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine whether either a peripheral nerve block under ultrasound (u/s) guidance of the lateral femoral cutaneous nerve (LFCN), versus an u/s guided block of the nerve followed by continuous catheter infusion of local anesthetic, offers better post-operative analgesia in pediatric burn patients undergoing reconstructive surgery, than the current analgesic regimen of subcutaneous local anesthetic infiltration. Eligible subject, pediatric patients having reconstructive surgery for burns, having skin graft donor sites of the lateral thighs, will be randomized into three groups: control (having local infiltration of site), ultrasound guided nerve block, or ultrasound guided nerve block with catheter placement --fascia iliac. Post-operative comfort will be assessed over the next 48 hours.
Conditions Studied
Interventions
- PROCEDURE Regional nerve block
- PROCEDURE Catheter
Study Locations (1)
Massachusetts
- Shriners Hospital for Children - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 19 participants |
| Start Date | 2008-04 |
| Est. Completion | 2013-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01500655
The ClinicalTrials.gov registry entry for NCT01500655 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 19 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 83-participant average among 36 other Burns trials with a reported enrollment target (77% lower). The listed sponsor is Massachusetts General Hospital, which has 2,032 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Burns appearing as the primary indexed condition, and to 2 interventions - of which Regional nerve block is the first listed.
NCT01500655 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT01500655 about?
NCT01500655 is a clinical study titled "Ultrasound-Guided Block of the Lateral Femoral Cutaneous Nerve in Pediatric Patients". The purpose of this study is to determine whether either a peripheral nerve block under ultrasound (u/s) guidance of the lateral femoral cutaneous nerve (LFCN), versus an u/s guided block of the nerve followed by continuous catheter infusion of local anesthetic, offers better post-operative analgesi...
What is the current status of trial NCT01500655?
This trial is currently completed. It is a NA study. The enrollment target is 19 participants. The study started on 2008-04. Estimated completion is 2013-09.
What conditions does trial NCT01500655 study?
This clinical trial studies the following conditions: Burns.
What interventions are being tested in trial NCT01500655?
The interventions under investigation include: Regional nerve block (PROCEDURE), Catheter (PROCEDURE).
Who is sponsoring clinical trial NCT01500655?
This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01500655 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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