Viewing Study NCT06373900



Ignite Creation Date: 2024-05-06 @ 8:25 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06373900
Status: COMPLETED
Last Update Posted: 2024-04-18
First Post: 2024-03-25

Brief Title: Wound Closure After Total Knee Arthroplasty Comparison of Polypropylene and Polyglactin 910 Suture
Sponsor: Indus Hospital and Health Network
Organization: Indus Hospital and Health Network

Study Overview

Official Title: Wound Closure After Total Knee Arthroplasty Comparison of Polypropylene and Polyglactin 910 Suture A Randomised Controlled Trial
Status: COMPLETED
Status Verified Date: 2024-04
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: None
Brief Summary: Comparison of wound complication and scar formation in patient undergone bilateral total knee replacement comparison between polypropylene and polyglactin 910 suture patient randomised according to SNOS protocol into group A and B for their right and left knee closure with each suture patient followed on 3rd 7th 15th and 30th post operative day for wound healing wound dehiscence and scar formation
Detailed Description: All patients aged 50-80 years belonging to either sex diagnosed with end-stage osteoarthritis or post-traumatic arthritis and scheduled for bilateral primary total knee arthroplasty at the Department of Orthopedics Indus Hospital and Health Network Karachi were enrolled in the study Exclusion criteria included patients having existing skin neuromuscular or connective tissue disorders rheumatoid arthritis immunosuppression morbid obesity and pregnancy All patients provided voluntary informed written consent before enrolment in the study

In all patients undergoing primary TKA one knee was closed using polypropylene whereas the other was closed with Polyglactin 910 sutures All surgeries were performed by the same surgical team using a standard medial parapatellar approach The number of sutures and wound closure techniques were standardized across both groups

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