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NCT02991404 · ClinicalTrials.gov registry record · Early Phase 1

Single Injection Adductor Canal Block Versus Continuous Adductor Canal Infusion for Total Knee Arthroplasty

A Early Phase 1 study of Pain, Postoperative and Total Knee Arthroplasty, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Early Phase 1
Development phase
60
Enrollment target
1
Study location

NCT02991404 is a Early Phase 1 study of Pain, Postoperative and Total Knee Arthroplasty that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 60 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02991404, a Early Phase 1 study of Pain, Postoperative and Total Knee Arthroplasty, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Early Phase 1
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

Patients undergoing Primary Total Knee Arthroplasty will be randomized to receive either multimodal single injection adductor canal block with sham infusion catheter or continuous infusion of local anesthetic (control) for postoperative analgesia. Primary end point is pain scores at 30 hours post performance of block procedure.

Interventions

  • PROCEDURE Multimodal Peripheral Nerve Block Injection
  • PROCEDURE Single Shot Adductor Canal Block
  • DRUG Initial Bolus
  • DRUG Continuous infusion

Study Locations (1)

North Carolina

  • Wake Forest Baptist Hospital - Winston-Salem

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2017-02-17
Est. Completion 2017-11-15
Phase Early Phase 1

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT02991404

The ClinicalTrials.gov registry entry for NCT02991404 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (78% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 4 interventions - of which Multimodal Peripheral Nerve Block Injection is the first listed.

NCT02991404 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT02991404 about?

NCT02991404 is a clinical study titled "Single Injection Adductor Canal Block Versus Continuous Adductor Canal Infusion for Total Knee Arthroplasty". Patients undergoing Primary Total Knee Arthroplasty will be randomized to receive either multimodal single injection adductor canal block with sham infusion catheter or continuous infusion of local anesthetic (control) for postoperative analgesia. Primary end point is pain scores at 30 hours post p...

What is the current status of trial NCT02991404?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 60 participants. The study started on 2017-02-17. Estimated completion is 2017-11-15.

What conditions does trial NCT02991404 study?

This clinical trial studies the following conditions: Pain, Postoperative, Total Knee Arthroplasty, Adductor Canal Block.

What interventions are being tested in trial NCT02991404?

The interventions under investigation include: Multimodal Peripheral Nerve Block Injection (PROCEDURE), Single Shot Adductor Canal Block (PROCEDURE), Initial Bolus (DRUG), Continuous infusion (DRUG).

Who is sponsoring clinical trial NCT02991404?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02991404 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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