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NCT01591603 · ClinicalTrials.gov registry record · NA
Comparison of Perineural Catheter Depth for the Continuous Popliteal Nerve Block Using Ultrasound Guidance and Dermabond
A NA study, sponsored by Vanderbilt University.
- Completed
- Registry status
- NA
- Development phase
- 83
- Enrollment target
NCT01591603 is a NA study that has completed, run by Vanderbilt University. The registered enrollment target is 83 participants.
The verdict
NCT01591603, a NA study, has completed, sponsored by Vanderbilt University.
- COMPLETED
- Registry status
- NA
- Development phase
- 83 participants
- Enrollment target
Study Summary
The study will investigate the difference in success rate between popliteal peripheral nerve catheters placed at 1 centimeter compared to 5 centimeters past the tip of a Tuohy needle.
Interventions
- PROCEDURE 1 cm
- PROCEDURE 5 cm
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 83 participants |
| Start Date | 2012-05 |
| Est. Completion | 2015-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01591603
The ClinicalTrials.gov registry entry for NCT01591603 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 83 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which 1 cm is the first listed.
NCT01591603 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01591603 about?
NCT01591603 is a clinical study titled "Comparison of Perineural Catheter Depth for the Continuous Popliteal Nerve Block Using Ultrasound Guidance and Dermabond". The study will investigate the difference in success rate between popliteal peripheral nerve catheters placed at 1 centimeter compared to 5 centimeters past the tip of a Tuohy needle.
What is the current status of trial NCT01591603?
This trial is currently completed. It is a NA study. The enrollment target is 83 participants. The study started on 2012-05. Estimated completion is 2015-07.
What interventions are being tested in trial NCT01591603?
The interventions under investigation include: 1 cm (PROCEDURE), 5 cm (PROCEDURE).
Who is sponsoring clinical trial NCT01591603?
This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.
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