Clinical Trials Directory

Trials / Completed

CompletedNCT05822973

Sutures for Treatment of Knee Arthroscopy

Absorbable Versus Nonabsorbable Sutures for the Treatment of Knee Arthroscopy: A Prospective Comparison of Patient Outcomes and Satisfaction

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
274 (actual)
Sponsor
Rothman Institute Orthopaedics · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

For a knee arthroscopy, two small incisions are made at the level of the joint line on each side of the patellar tendon. Closure of surgical incisions consists of using either nonabsorbable or absorbable sutures. Some surgeons prefer using nonabsorbable sutures due to it being easier to tie, these sutures are less likely to break prematurely, and that they elicit a minimal inflammatory response. On the other hand, some surgeons prefer using absorbable sutures due to the time savings of not having to remove the sutures at a later date and that these sutures decrease patient anxiety and discomfort. The purpose of this study is to prospectively investigate and compare patient's pain, swelling and cosmesis following knee arthroscopy surgery between patients who had their arthroscopy portals closed using resorbable sutures vs. patients who had their portals closed using nonabsorbable sutures.

Conditions

Interventions

TypeNameDescription
DEVICE3.0 monocryl sutureincision will be closed with absorbable suture
DEVICE3.0 nylon sutureincision will be closed with non-absorbable suture

Timeline

Start date
2018-11-18
Primary completion
2023-04-09
Completion
2023-04-09
First posted
2023-04-21
Last updated
2023-04-21

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05822973. Inclusion in this directory is not an endorsement.