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NCT01711307: AchillesRCT

Operative vs. Non-Operative Treatment of Acute Ruptures of the Achilles Tendon

Terminated NA Last updated 9 July 2020
What this trial tests

NA trial testing operative in Ruptured Achilles Tendon in 220 participants. Terminated before completion.

Timeline
1 October 2012
Primary endpoint
31 December 2019
30 June 2020

Quick facts

Lead sponsorMark Glazebrook
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment220
Start date1 October 2012
Primary completion31 December 2019
Estimated completion30 June 2020
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Mark Glazebrook

Who can join

18 and older, any sex, with Ruptured Achilles Tendon. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The proposed trial is a multi-centre prospective randomized controlled trial comparing outcomes of patients with acute Achilles tendon ruptures treated either non-operatively or with open operative tendon repair. All patients will undergo accelerated functional rehabilitation. The primary outcome measure is Achilles tendon re-rupture rate.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01711307.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing