CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 47 enrolled
Drug / intervention
Blood Flow Restriction using Delfi Personalized Tourniquet Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04285879
NCT04285879N/ACompleted

A Determination of Efficacy and Therapeutic Benefits of Blood Flow Restriction Training in an Adolescent Population

Connecticut Children's Medical Center·interventional·Posted Feb 26, 2020·Updated Jul 17, 2024

In Brief

A clinical study evaluating Blood Flow Restriction using Delfi Personalized Tourniquet System for Blood Flow Restriction and 2 related conditions. Completed, enrolled 47 participants across 1 site.

Detailed Summary

While there are a number studies that have reported on the use of BFR in the adult population, there is limited information about the use of BFR in the adolescent population. This study aims to evaluate the use of BFR training in conjunction with traditional ACL (anterior cruciate ligament) reconstruction rehabilitation in adolescents. The purpose of this study is to evaluate the addition of BFR-based exercise to traditional methods of physical therapy. Does the use of BFR-based exercise improve strength, hypertrophy, functional and patient reported outcomes after ACL Reconstruction in the adolescent population?

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedFeb 26, 2020
Enrollment StartDec 15, 2020
Primary CompletionJan 15, 2023
Study CompletionOct 16, 2023
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 6.4 years ago

Interventions

Blood Flow Restriction using Delfi Personalized Tourniquet Systemdevice

The Delfi Tourniquet System is designed to be used in conjunction with exercise. The system automatically determines the degree of occlusion and allows for safe regulation of pressure. Patients will then complete exercises with the use of this device following the Owens Recovery Science Protocol