Viewing Study NCT04865692



Ignite Creation Date: 2024-05-06 @ 4:05 PM
Last Modification Date: 2024-10-26 @ 2:03 PM
Study NCT ID: NCT04865692
Status: COMPLETED
Last Update Posted: 2021-04-29
First Post: 2021-04-26

Brief Title: Effects of Low Intensity Blood Flow Restriction on Clinical Outcomes in Women With Knee Osteoarthritis
Sponsor: University of Lahore
Organization: University of Lahore

Study Overview

Official Title: Effects of Blood Flow Restriction on Clinical Outcomes in Women With Knee Osteoarthritis
Status: COMPLETED
Status Verified Date: 2021-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: BFR
Brief Summary: Objective is to compare the effects of routine physical therapy with and without low intensity blood flow restriction on pain and quadriceps muscle strength in women with knee osteoarthritis

A single blinded randomized controlled trial conducted at Department of Physiotherapy University of Lahore Teaching Hospital Defense Road Lahore

Total 60 participants were randomly assigned in to two groups with 30 in each group The intervention group received routine physiotherapy program combined with Low Intensity Blood Flow Restriction Technique LI-BFR While control group were treated with only routine physiotherapy

Dynamometer was used to assess the knee extensor strength while Knee injury and osteoarthritis outcome score was used to record any exacerbation in pain and effects of BFR on activities of daily living Training load determined 20 of 1RM Data analysis had done on SPSS version 23
Detailed Description: nonparametric test Friedman test was for comparison within the groups and Mann Whitney U test was used for comparison between groups

Randomization had done through the sealed envelope method After allocation subjects had received their treatment protocals

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None