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NCT03746951 · ClinicalTrials.gov registry record · Phase 2
Comparative Evaluation of Lumbar Plexus and Suprainguinal Fascia Iliaca Compartment Blocks
A Phase 2 study, sponsored by Nationwide Children's Hospital.
- Completed
- Registry status
- Phase 2
- Development phase
- 15
- Enrollment target
NCT03746951: Completed Phase 2 study, sponsored by Nationwide Children's Hospital.
NCT03746951 is a Phase 2 study that has completed, run by Nationwide Children's Hospital. The registered enrollment target is 15 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03746951, a Phase 2 study, has completed, sponsored by Nationwide Children's Hospital.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 15 participants
- Enrollment target
Study Summary
The investigators aim to compare the use of a suprainguinal fascia iliaca compartment block vs lumbar plexus block as an adjunct to general anesthesia in pediatric patients undergoing orthopedic procedures involving the hip or upper femur. This study will help determine the efficacy of the two techniques and their advantages when compared to each other including time to perform the block, opioid consumption reduction, effects on postoperative pain, and the length of stay.
Primary Outcome
The amount of time if takes to perform either the FICB or LPB.
Interventions
- DRUG Ropivacaine Hcl 0.5% Inj Vil 20Ml
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2019-04-24 |
| Est. Completion | 2020-01-31 |
| Phase | Phase 2 |
What the finished NCT03746951 record still lists
NCT03746951 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower).
The record links to 0 conditions, and to 1 intervention - of which Ropivacaine Hcl 0.5% Inj Vil 20Ml is the first listed.
NCT03746951 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03746951 about?
NCT03746951 is a clinical study titled "Comparative Evaluation of Lumbar Plexus and Suprainguinal Fascia Iliaca Compartment Blocks". The investigators aim to compare the use of a suprainguinal fascia iliaca compartment block vs lumbar plexus block as an adjunct to general anesthesia in pediatric patients undergoing orthopedic procedures involving the hip or upper femur. This study will help determine the efficacy of the two techn...
What is the current status of trial NCT03746951?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 15 participants. The study started on 2019-04-24. Estimated completion is 2020-01-31.
What interventions are being tested in trial NCT03746951?
The interventions under investigation include: Ropivacaine Hcl 0.5% Inj Vil 20Ml (DRUG).
Who is sponsoring clinical trial NCT03746951?
This trial is sponsored by Nationwide Children's Hospital, which has 188 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03746951's enrollment target sits among peer trials
15 1919th of 2000 higher than 60 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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