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Ensayo clínico

Werewolf Flow 50 During ACL Reconstruction

NCT: NCT04998656 · COMPLETED

ID NCTNCT04998656
EstadoCOMPLETED
Fecha de inicio2021-07-12
Finalización2024-11-02
SponsorUniversity of Colorado, Denver (OTHER)
First posted
Last updated

Resumen breve

The aim of this study is to compare the outcomes, ease of use, and cost of the Werewolf FLOW50 device to the institutional standard of care which is does not include the use of electrocautery devices during anterior cruciate ligament reconstruction (ACLR) surgery in patients 12-18 years of age using a randomized control trial design. The investigators hypothesize that a lower proportion of participants who undergo ACLR and are randomized to the Werewolf FLOW50 procedure will experience post-operative arthrofibrosis compared to those randomized to standard of care (control group).

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.

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