Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure

Part of paid clinical trials in Columbia, Missouri.

Sponsor
University of Missouri-Columbia
Study ID
NCT06845735
Status
Recruiting

Conditions

  • Femoroacetabular Impingement Syndrome
  • Hip Arthroscopy
  • Labrum Injury of the Hip Joint

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Non-Absorbable Sutures — DEVICE
    Non-Absorbable Sutures
  • Absorbable Suture — DEVICE
    Absorbable suture

Study Details

The study is to prospectively compare absorbable sutures with non-absorbable sutures used for capsular repair during hip arthroscopic procedures. Major outcomes will be measured using three questionnaires ((1) International Hip Outcome Tool-12 (iHOT-12), (2) modified Harris hip score, (3) hip outcome score) in addition to the standard of care set of 9 questionnaires. The other major outcome will be any radiographic heterotrophic ossification at the 6-month follow-up time point.

Key Dates

Start date
Mar 22, 2024
Status verified
Apr 2025
Primary completion
Jan 1, 2028
Completion
Jan 1, 2028

Study Design

Enrollment
100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Absorbable Suture
    Absorbable suture
  • Active Comparator: Non-Absorbable Suture
    Non-Absorbable Sutures

Primary Outcome Measure

International Hip Outcome Tool-12 (IHOT-12) [ Time Frame: Preoperative to 12 months postoperative ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Missouri Orthopaedic InstituteColumbiaMissouri65201
Vicki Jones, MEd, CCRP
573-882-7583
Steven F DeFroda, MD, MEng (PRINCIPAL_INVESTIGATOR)

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