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NCT02453321 · ClinicalTrials.gov registry record · Phase 4

Continuous Adductor Canal Blocks Vs. Low Dose Femoral Nerve Blocks For Early Rehabilitation After Total Knee Arthroplasty

A Phase 4 study of Pain, Postoperative and Total Knee Arthroplasty (TKA), sponsored by Kevin King, DO.

Completed
Registry status
Phase 4
Development phase
62
Enrollment target
1
Study location

NCT02453321: Completed Phase 4 study of Pain, Postoperative and Total Knee Arthroplasty (TKA), sponsored by Kevin King, DO.

NCT02453321 is a Phase 4 study of Pain, Postoperative and Total Knee Arthroplasty (TKA) that has completed, run by Kevin King, DO. The registered enrollment target is 62 participants, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (77% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02453321, a Phase 4 study of Pain, Postoperative and Total Knee Arthroplasty (TKA), has completed, sponsored by Kevin King, DO.

COMPLETED
Registry status
Phase 4
Development phase
62 participants
Enrollment target
1
Study location

Study Summary

Recently, several articles have suggested or reported that Adductor Canal Blocks (ACBs) offer adequate or equal analgesia and may promote better performance in early rehabilitation following Total Knee Arthroplasty (TKA) when compared to the more commonly used Femoral Nerve Block (FNB). A common feature of these studies has been the use of moderate to high concentration local anesthetics (e.g. 0.2% or 0.5% Ropivacaine respectively) which when injected by a large motor nerve will inevitably cause weakness. However, the practice at our institution has long been a continuous femoral nerve block (CFNB) with a lower concentration local anesthetic (0.0625% Bupivacaine). Over the past several years the investigators have performed several thousand CFNBs using this technique which has offered the advantage of minimal motor weakness and adequate analgesia. The primary goal of this study is to determine if our established practice of using a low concentration continuous FNB inserted about 5cm caudal to the groin crease (the apex of the femoral triangle) using a low infusion rate of 2ml/hr is comparable to the emerging practice of inserting a Continuous Peripheral Nerve Block (CPNB) in the anatomic adductor canal (AC) - infusing at 4ml/hr. A secondary goal is to study the effect of cumulative volume of local anesthetic infused through a FNB when at a rate of 2ml/hr compared to a rate of 4ml/hr in the 48-hour postoperative period. Definitions of the location of the adductor canal are debated heavily in literature, but they seem to agree that the middle 1/3 of the thigh contains the proximal AC while the distal 1/3 of the thigh contains the adductor hiatus - the terminal end of the AC. Our study will require placement of the continuous ACB no more distal than 20cm cephalad to the superior pole of the patella due to placement prior to surgery and the need to keep the dressing out of the operative field. The CACB catheter will also not be placed any more proximal than 20cm dista

Primary Outcome

Ability to walk 75 feet if performed on POD#2 is usually considered the main criterion for discharge at UPMC Passavant. The patient is accompanied/supervised by physical therapist using a walker but without active intervention by therapist, unless necessary. The earliest day on which the patient achieves the 75-feet unassisted walk will be recorded for comparison among the arms/groups.

Interventions

  • DRUG Bupivacaine
  • PROCEDURE Continuous Femoral Nerve Block
  • PROCEDURE Nerve Block, Continuous Adductor Canal
  • PROCEDURE Continuous Sciatic Nerve Block

Study Locations (1)

Pennsylvania

  • University of Pittsburgh Medical Center - Passavant Hospital - Pittsburgh

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2015-06
Est. Completion 2016-08-31
Phase Phase 4
Kevin King, DO

1 total trials

What the finished NCT02453321 record still lists

NCT02453321 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 62 participants, a relatively small participant target, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (77% lower).

The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 4 interventions - of which Bupivacaine is the first listed.

NCT02453321 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02453321 about?

NCT02453321 is a clinical study titled "Continuous Adductor Canal Blocks Vs. Low Dose Femoral Nerve Blocks For Early Rehabilitation After Total Knee Arthroplasty". Recently, several articles have suggested or reported that Adductor Canal Blocks (ACBs) offer adequate or equal analgesia and may promote better performance in early rehabilitation following Total Knee Arthroplasty (TKA) when compared to the more commonly used Femoral Nerve Block (FNB). A common fea...

What is the current status of trial NCT02453321?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 62 participants. The study started on 2015-06. Estimated completion is 2016-08-31.

What conditions does trial NCT02453321 study?

This clinical trial studies the following conditions: Pain, Postoperative, Total Knee Arthroplasty (TKA).

What interventions are being tested in trial NCT02453321?

The interventions under investigation include: Bupivacaine (DRUG), Continuous Femoral Nerve Block (PROCEDURE), Nerve Block, Continuous Adductor Canal (PROCEDURE), Continuous Sciatic Nerve Block (PROCEDURE).

Who is sponsoring clinical trial NCT02453321?

This trial is sponsored by Kevin King, DO, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02453321 being conducted?

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

Similar trials for Pain, Postoperative

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02453321's enrollment target sits among peer trials

62 77th of 113 higher than 36 of 113 other Pain, Postoperative trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pain, Postoperative 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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Source: ClinicalTrials.gov NCT02453321, the US trial registry maintained by the National Library of Medicine. NCT02453321 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.