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Sutures for Treatment of Knee Arthroscopy

Rothman Institute Orthopaedics logo

Rothman Institute Orthopaedics

Status

Completed

Conditions

Suture
Knee Arthroscopy

Treatments

Device: 3.0 monocryl suture
Device: 3.0 nylon suture

Study type

Interventional

Funder types

Other

Identifiers

NCT05822973
KFRE18D.721

Details and patient eligibility

About

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.

Enrollment

274 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients ages 18 and older undergoing primary knee arthroscopy for diagnostic arthroscopy, removal of a loose body, chondroplasty, or a partial meniscectomy will be included in this analysis

Exclusion criteria

  • Patients undergoing revision knee arthroscopy as well as patients undergoing ACL reconstruction or meniscal repair surgery will be excluded from this analysis.
  • Patients under the age of 18 will be excluded as well.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

274 participants in 2 patient groups

would closure using absorbable sutures
Active Comparator group
Description:
patients randomized into the absorbable suture group will have their incisions closed with 3.0 monocryl sutures
Treatment:
Device: 3.0 monocryl suture
would closure using non-absorbable sutures
Active Comparator group
Description:
Patients randomized into the nonabsorbable suture group will have their incisions closed with either a 3.0 nylon suture
Treatment:
Device: 3.0 nylon suture

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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