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Virtual Reality Rehabilitation for Patients With Anterior Cruciate Ligament Reconstruction - Trial NCT05080894

Access comprehensive clinical trial information for NCT05080894 through Pure Global AI's free database. This phase not specified trial is sponsored by Institut d'Investigacions Biomรจdiques August Pi i Sunyer and is currently Recruiting. The study focuses on Knee Injuries. Target enrollment is 44 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.gov โ€ข NCT05080894
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Virtual Reality Rehabilitation for Patients With Anterior Cruciate Ligament Reconstruction
Early Domestic Rehabilitation Using Virtual Reality for Patients With Anterior Cruciate Ligament Reconstruction: a Randomized Controlled Trial

Study Focus

Knee Injuries

Virtual reality

Interventional

device

Sponsor & Location

Institut d'Investigacions Biomรจdiques August Pi i Sunyer

Barcelona, Spain

Timeline & Enrollment

N/A

Oct 01, 2021

Mar 15, 2023

44 participants

Primary Outcome

The International Knee Documentation Committee (IKDC) Subjective Knee Form,The International Knee Documentation Committee (IKDC) Subjective Knee Form,The International Knee Documentation Committee (IKDC) Subjective Knee Form,The International Knee Documentation Committee (IKDC) Subjective Knee Form

Summary

The purpose of this study is to ascertain whether 4 weeks of daily virtual-reality-based
 rehabilitation at home improves disability in the early stages of recovery from anterior
 cruciate ligament reconstruction surgery compared with standard care.

ICD-10 Classifications

Injuries to the knee and lower leg
Sprain and strain of other and unspecified parts of knee
Other spontaneous disruption of ligament(s) of knee
Crushing injury of knee
Injury to multiple structures of knee

Data Source

ClinicalTrials.gov

NCT05080894

Device Trial