Viewing Study NCT06172231



Ignite Creation Date: 2024-05-06 @ 7:54 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06172231
Status: RECRUITING
Last Update Posted: 2023-12-15
First Post: 2023-12-07

Brief Title: Effects of Instrument Assisted Soft Tissue Mobilization in Addition to Conventional Physiotherapy in Knee Arthrofibrosis
Sponsor: Foundation University Islamabad
Organization: Foundation University Islamabad

Study Overview

Official Title: Effects of Instrument Assisted Soft Tissue Mobilization in Addition to Conventional Physiotherapy in Knee Arthrofibrosis
Status: RECRUITING
Status Verified Date: 2023-12
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: Arthrofibrosis is the abnormal proliferation of fibrous tissue within a joint and around the joint that leads to loss of motion pain muscle weakness swelling functional limitation Study conducted to determine additional effects of IASTM along with conventional physiotherapy as compared to conventional physiotherapy alone on Range of motion functional limitation and pain in knee arthrofibrosis
Detailed Description: Arthrofibrosis is common condition after surgeries most of the arthrofibrosis literature addresses arthrofibrosis after arthroplasty or ligamentous reconstruction and it is replete with manipulation under anesthesia or with arthroscopic interventions or both Study will be conducted over period of 1 year at fauji foundation hospitalEthical approval from ERC foundation university medical college Participants recruited and written inform consent following which they will be required to complete a self-reported demographic form The data will be entered and analyzed on SPSS 22 IASTM is simple and effective intervention to improve Rom and functional limitation in patients with knee arthrofibrosis

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