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NCT02380183 · ClinicalTrials.gov registry record · NA

Needle-Guided vs Free-Hand Technique in Performing Brachial Plexus Blockade

A NA study, sponsored by Montefiore Medical Center.

Completed
Registry status
NA
Development phase
70
Enrollment target

NCT02380183 is a NA study that has completed, run by Montefiore Medical Center. The registered enrollment target is 70 participants.

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The verdict

NCT02380183, a NA study, has completed, sponsored by Montefiore Medical Center.

COMPLETED
Registry status
NA
Development phase
70 participants
Enrollment target

Study Summary

This is an openly randomized controlled parallel group study evaluating the effectiveness of using a guided approach and free-hand approach in performing upper extremity regional blocks. Potential subjects for this study are the patients who are scheduled for upper extremity surgeries requiring supraclavicular and interscalene brachial plexus blocks at Montefiore Medical Center. Rotating residents who are participating in the study will be randomly assigned either to perform block under guided approach (with the help of needle guidance) or free-hand without the needle guidance. All the blocks will be single injection blocks utilizing the in-plane technique for needle insertion which is the usual protocol in our institution. Each resident will be performing one interscalene block with the device and one without the device and one supraclavicular block with device and one without the device. An independent observer will be present during the case and will be responsible for recording the time taken to perform the block, number of times the needle has been redirected and the number of times the needle is reinserted. This observer will also administer the satisfaction questionnaire. Number of time needle is redirected and number of times reinserted is also a self reported assessment by the physician who is performing the block. Efficacy of the block will be assessed by the standard of care practiced at our center.

Interventions

  • DEVICE Civco Needle Guidance Device

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2014-10
Est. Completion 2015-06
Phase NA

Sponsor

Montefiore Medical Center

345 total trials

What the Registry Record Tells You About NCT02380183

The ClinicalTrials.gov registry entry for NCT02380183 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Montefiore Medical Center, which has 345 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Civco Needle Guidance Device is the first listed.

NCT02380183 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02380183 about?

NCT02380183 is a clinical study titled "Needle-Guided vs Free-Hand Technique in Performing Brachial Plexus Blockade". This is an openly randomized controlled parallel group study evaluating the effectiveness of using a guided approach and free-hand approach in performing upper extremity regional blocks. Potential subjects for this study are the patients who are scheduled for upper extremity surgeries requiring supr...

What is the current status of trial NCT02380183?

This trial is currently completed. It is a NA study. The enrollment target is 70 participants. The study started on 2014-10. Estimated completion is 2015-06.

What interventions are being tested in trial NCT02380183?

The interventions under investigation include: Civco Needle Guidance Device (DEVICE).

Who is sponsoring clinical trial NCT02380183?

This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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