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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01376024
Other study ID # AAAC0826
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 2, 2007
Est. completion date August 31, 2025

Study information

Verified date June 2024
Source Columbia University
Contact Bryanna Geiger
Phone 212-305-3912
Email bg2603@columbia.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The data in this prospective registry will be used 1) to define which surgical and nonoperative techniques are most effective at providing pain relief, restoring function, are cost effective, and patients are satisfied with their outcomes; and 2) to design focused clinical questions regarding the optimal treatment of basal joint arthritis of the thumb in future randomized controlled trials. There are no interventions or changes in patient care associated with this study.


Description:

Basal joint arthritis of the thumb is a common condition associated with considerable morbidity. Many non-operative and operative treatments have been described but few multi-center prospective evidence based trials comparing standard treatments have been done. This continuing search for consensus of best clinical practices has been reviewed in a thorough meta-analysis of operative treatments for basal joint arthritis. Through the systematic collection of data regarding patient-specific characteristics, treatment interventions, and longitudinal functional outcome measurements the investigators believe patient outcomes and satisfaction can improve through the elucidation of risk factors for disease progression, and the timing and selection of treatment modalities, either conservative or surgical, for any particular patient. The establishment of a multi-center clinical registry will greatly facilitate these goals. The study hypothesizes that there exist effective non-operative and operative treatments for certain patient populations with basal joint arthritis of the thumb. There also exists a functionally superior, cost effective, and low risk non-operative or minimally invasive operative treatment regime to alleviate pain and slow the progression of disease in those with less advanced disease. Likewise, there is significant functional, health utility, and economic advantage to surgically treating advanced basal joint arthritis with one of the popularized procedures currently in practice.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date August 31, 2025
Est. primary completion date August 31, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who have symptomatic basal joint arthritis. - Patients who are capable of providing informed consent. Exclusion Criteria: - Patients younger than 18 years old at the time of enrollment. - Patients with neuromuscular disease affecting the operated hand, not caused by the CMC operation. - Patients with known inflammatory arthritic conditions, such as rheumatoid or psoriatic arthritis. - Patients with a history of or current infection of the basal joint of the affected hand. - Patients who are demented or are unable to provide informed consent. - Patients unable to comply with study guidelines. - Patients who have metacarpophalangeal joint hyperextension are NOT excluded. These patients will be followed and if they receive a capsulodesis or other procedure at the MCPJ at the same time as their basal joint arthroplasty this will be noted in their data records.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Vanderbilt University Hospital Nashville Tennessee
United States Columbia University/NY Presbyterian Hospital New York New York
United States Mayo Clinic Rochester Minnesota

Sponsors (2)

Lead Sponsor Collaborator
Columbia University Orthopedic Research and Education Foundation

Country where clinical trial is conducted

United States, 

References & Publications (1)

Martou G, Veltri K, Thoma A. Surgical treatment of osteoarthritis of the carpometacarpal joint of the thumb: a systematic review. Plast Reconstr Surg. 2004 Aug;114(2):421-32. doi: 10.1097/01.prs.0000131989.86319.b1. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Flexion/extension range of MCP joint Range of motion measured in degrees of the metacarpophalangeal (MCP) joint. Baseline, 6 weeks, 3 months, 6 months, 1 year
Primary Flexion/extension range of IP joint Range of motion measured in degrees of the interphalangeal (IP) joint. Baseline, 6 weeks, 3 months, 6 months, 1 year
Primary Grip strength This will be quantified with use of a Jamar dynamometer set in the second position. Baseline, 6 weeks, 3 months, 6 months, 1 year
Primary Key-pinch strength A 30-lb pinch dynamometer will used to determine lateral key-pinch strength. Baseline, 6 weeks, 3 months, 6 months, 1 year
Primary Tip-pinch strength A 30-lb pinch dynamometer will used to determine lateral tip-pinch strength. Baseline, 6 weeks, 3 months, 6 months, 1 year
Secondary Average total costs per patient Review or estimation of hospital and office bills including those for the prescribed therapy and/or splinting will be tallied for each patient. Up to 1 year
Secondary Disability of Arm, Shoulder and Hand (DASH) score A questionnaire designed to assess musculoskeletal disorders of the upper limbs. Baseline, 6 weeks, 3 months, 6 months, 1 year
Secondary SF-36 questionnaire score A questionnaire designed to validate general health: surveys physical functioning, performance in a physical role, performance in an emotional role, vitality, social functioning, bodily pain, general health perceptions, and mental health. Baseline, 6 weeks, 3 months, 6 months, 1 year
Secondary Prevalence of arthritis progression Radiographs will be performed classify each patient within the Eaton 102 osteoarthritis staging system. Sequential radiographs will be examined for progression of joint abnormalities. Baseline, 6 weeks, 3 months, 6 months, 1 year
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