Viewing Study NCT06420648



Ignite Creation Date: 2024-06-16 @ 11:47 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06420648
Status: RECRUITING
Last Update Posted: 2024-06-06
First Post: 2024-05-14

Brief Title: Controlled Active Motion vs Early Passive Mobilization for Flexor Tendons Repair
Sponsor: University of Hail
Organization: University of Hail

Study Overview

Official Title: A Randomized Controlled Trial Comparing Controlled Active Motion and Early Passive Mobilization Protocols for Rehabilitation of Repaired Flexor Tendons in Zone II
Status: RECRUITING
Status Verified Date: 2024-06
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: None
Brief Summary: a randomized controlled trial tends to compare 2 rehabilitation approaches - early passive mobilization EPM and controlled active motion CAM - that are commonly used in the treatment of post-surgical flexor tendon repair of the hand
Detailed Description: a randomized controlled trial tends to compare 2 rehabilitation approaches commonly used in the treatment of post-surgical flexor tendon repair of the hand in this study the authors try to fill the gap in the literature regarding the more effective approach the comparisons between both approaches were scarce in previous literature

Participants will be randomly allocated to one of two treatment groups early passive mobilization EPM using a modified Kleinert protocol or controlled active motion CAM using a modified Duran technique n20 Patients were assessed at baseline and then at the 6th and 12th weeks of interventions to quantify total active motion TAM of the proximal and distal interphalangeal joints using goniometry and grip strength with dynamometry the disability level will be assessed using the Disabilities of the Arm Shoulder and Hand DASH questionnaire

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