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Acute Achilles Repair With or Without OrthADAPT Augmentation | Clinical Trials | Clareo Health

WITHDRAWNNANCT00962143

Acute Achilles Repair With or Without OrthADAPT Augmentation

The purpose of this study is to assess the clinical performance of the OrthADAPT Bioimplant in patients with acute mid-substance Achilles tendon tears requiring surgical repair.

Lead sponsor: Baxter Healthcare Corporation•1 U.S. locations•View source on ClinicalTrials.gov

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Trial snapshot

StatusWITHDRAWN

PhaseNA

Enrollment—

Start dateJun 2008

Last updatedApr 5, 2017

Condition

Achilles Tendon Tear

Locations shown

Orthopaedic Institute of Central Jersey

Sea Girt, New Jersey

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 5, 2017Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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