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Purpose

This study plans to learn more about the effect of adding tissue graft for wrist osteoarthritis reconstruction procedures. Previous studies have shown better allograft stability, and no documented foreign body reaction than with silicone and other synthetic materials.

Condition

Eligibility

Eligible Ages
Between 30 Years and 80 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • symptomatic wrist arthritis associated with SLAC or SNAC pathology - Patients 30 years or older or 80 years or younger

Exclusion Criteria

  • Patients younger than 29 years or older than 80 years - History of previous surgery related to wrist osteoarthritis

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group Assignment
Primary Purpose
Treatment
Masking
Single (Participant)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Meniscal Allograft with PRC 		These patients will receive a tissue allograft with their wrist reconstruction procedure.
  • Procedure: Meniscus Allograft Transplantation with Proximal Row Carpectomy
    Supplementing the wrist reconstruction with a meniscal allograft to improve wrist function and pain scores.
Placebo Comparator
PRC only 		These patients will receive the standard proximal row carpectomy procedure.
  • Procedure: Proximal Row Carpectomy
    Standard proximal row carpectomy with no tissue or synthetic adjuncts

Recruiting Locations

UCHealth Steadman Hawkins Clinic Inverness
Englewood, Colorado 80112
Contact:
Emma Judge
720-872-4850
emma.judge@cuanschutz.edu

More Details

Status
Recruiting
Sponsor
University of Colorado, Denver

Study Contact

Fraser J Leversedge, MD
919-316-0616
fraser.leversedge@cuanschutz.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.