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Recruiting NCT05412615

PRC With Meniscal Allograft Arthroplasty for Wrist Osteoarthritis

No phase Interventional Wrist Osteoarthritis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Meniscus Allograft Transplantation with Proximal Row Carpectomy, Proximal Row Carpectomy.
Who it may be relevant to
Registry conditions: Wrist Osteoarthritis. Basic parameters: 30 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Proximal Row Carpectomy With Meniscal Allograft Arthroplasty for Wrist Osteoarthritis

Overview

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.

Interventions

  • Procedure Meniscus Allograft Transplantation with Proximal Row Carpectomy
    Supplementing the wrist reconstruction with a meniscal allograft to improve wrist function and pain scores.
  • Procedure Proximal Row Carpectomy
    Standard proximal row carpectomy with no tissue or synthetic adjuncts

Primary outcome measures

  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: Baseline/Pre-op [Time frame: Preoperatively]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 2 weeks [Time frame: 2 weeks]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 6 weeks [Time frame: 6 weeks]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 3 months [Time frame: 3 months]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 6 months [Time frame: 6 months]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 9 months [Time frame: 9 months]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 12 months [Time frame: 12 months]
  • DISABILITIES OF THE ARM, SHOULDER AND HAND Score: 24 months [Time frame: 24 months]
Secondary outcome measures (3)
  • Pain Score [Time frame: Preoperatively, up to 24 Months]
  • Radiographic joint spacing [Time frame: 3 months, up to 24 Months]
  • MRI Joint Spacing [Time frame: 9 Months, 24 Months]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Single group
Masking
Single blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • UCHealth Steadman Hawkins Clinic Inverness — Englewood

Identifiers

NCT: NCT05412615 · 21-3148

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗