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NCT03285529 · ClinicalTrials.gov registry record · NA

The Use of STRATAFIX Suture Device Compared to Standard-of-care for Deep Tissue Closure in Total Knee Arthroplasty

A NA study, sponsored by The Cleveland Clinic.

Completed
Registry status
NA
Development phase
60
Enrollment target

NCT03285529: Completed NA study, sponsored by The Cleveland Clinic.

NCT03285529 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03285529, a NA study, has completed, sponsored by The Cleveland Clinic.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

The STRATAFIX (Ethicon, Johnson and Johnson, Somerville, New Jersey) Knotless Tissue Control suture device is a barbed suture that uses anchor technology to securely engage with the soft tissues while also eliminating the need for knots. The anchors, or barbs, are pressed out of the device core or formed within the core in a geometric pattern and arranged in a tapered manner to allow the device to pass through tissue in the direction toward the needle during closure. These knotless tissue control devices are deployed using a continuous technique, which is anticipated to be faster and more cost-effective than interrupted suturing.

Primary Outcome

Time from first needle insertion to complete skin closure per protocol

Interventions

  • DEVICE STRATIFIX
  • DEVICE VICRYL

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2017-09-26
Est. Completion 2019-05-31
Phase NA
The Cleveland Clinic

688 total trials

What the finished NCT03285529 record still lists

NCT03285529 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which STRATIFIX is the first listed.

NCT03285529 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03285529 about?

NCT03285529 is a clinical study titled "The Use of STRATAFIX Suture Device Compared to Standard-of-care for Deep Tissue Closure in Total Knee Arthroplasty". The STRATAFIX (Ethicon, Johnson and Johnson, Somerville, New Jersey) Knotless Tissue Control suture device is a barbed suture that uses anchor technology to securely engage with the soft tissues while also eliminating the need for knots. The anchors, or barbs, are pressed out of the device core or f...

What is the current status of trial NCT03285529?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2017-09-26. Estimated completion is 2019-05-31.

What interventions are being tested in trial NCT03285529?

The interventions under investigation include: STRATIFIX (DEVICE), VICRYL (DEVICE).

Who is sponsoring clinical trial NCT03285529?

This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03285529's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT03285529, the US trial registry maintained by the National Library of Medicine. NCT03285529 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.