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A Case Series Comparing T+LRTI to Partial Trapeziectomy for Thumb Osteoarthritis

Measuring the Quality of Life in Patients Receiving a Partial Trapeziectomy (PT) Using a Minimalist Approach Versus a Complete Trapeziectomy With Ligament Reconstruction and Tendon Interposition (T+LRTI)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03392454
Enrollment
20
Registered
2018-01-08
Start date
2012-03-01
Completion date
2015-11-30
Last updated
2024-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Health Related Quality of Life, Osteoarthritis

Keywords

Partial Trapeziectomy, Tendon Interposition, Trapeziectomy, Thumb Carpometacarpal Joint

Brief summary

The purpose of this study was to measure the differences in Health Related Quality of Life (HRQOL) and functional measurements between two groups of patients with Carpometacarpal Osteoarthritis of the thumb.

Detailed description

Two patient groups, who have been diagnosed with Carpometacarpal Osteoarthritis of the thumb were compared to measure the Health Related Quality of life (HRQOL) and functional outcomes following two different surgical procedures. The first procedure is currently the most used procedure is North America, Trapeziectomy with Ligament Reconstruction and Tendon Interposition (T+LRTI); this procedure is compared to Partial Trapeziectomy and Tendon Interposition (PT+TI). HRQOL is measured using three questionnaires: one generic, one condition specific and one to measure utility (costs). Patients received their procedures from the respective surgeons and then came in for regular follow up at 1, 3, 6 and 12 months. At these follow up visits the questionnaires and functional measurements (including grip, key pinch and tip pinch strength), were completed

Interventions

PROCEDURET+LRTI

T+LRTI is the most commonly used procedure, it removes the entire trapezium

PROCEDUREPT+TI

The PT+TI is less invasive than the T+LRTI as only part of the trapezium is removed

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of advanced stage (Eaton stages II-IV) Carpometacarpal joint (CMCJ) osteoarthritis (OA of the thumb * Willingness to undergo surgery for CMCJ OA; * Over the age of 18; * Able to provide informed consent; and * Ability to read and comprehend English to complete the HRQOL questionnaires

Exclusion criteria

* 1\) Diagnosis of Eaton stage I CMCJ OA of the thumb \[17\]; 2) Under the age of 18; 3) Presence of any concomitant hand pathology (including rheumatoid arthritis, neuropathy and traumatic arthritis); and 4) Previous surgery on the same hand or currently under consideration for other unrelated hand surgery

Design outcomes

Primary

MeasureTime frameDescription
Change in Health Related Quality of Life (HRQOL) as measured by the Short Form 36v2 (SF-36)1 week pre-operatively plus 1, 3, 6 and 12 month post-operativelyThe Short-Form 36v2 \[SF-36\] is a Generic HRQOL questionnaire
Change in Health Related Quality of Life (HRQOL) as measured by the Disabilities of the Arm, Shoulder and Hand (DASH)1 week pre-operatively plus 1, 3, 6 and 12 month post-operativelyThe DASH is a condition specific questionnaire
Change in HRQOL as measured by The EuroQol-5D-3L [EQ-5D]1 week pre-operatively plus 1, 3, 6 and 12 month post-operativelyThe EQ-5D is a questionnaire that allows utility to be calculated

Secondary

MeasureTime frameDescription
Change in functional performance as measured by Grip Strength1 week pre-operatively and 3, 6 and 12 month post-operativelyForce applied by the hand, measured by a goniometer in kilograms
Change in functional performance as measured by Two-Point Pinch Strength1 week pre-operatively and 1, 3, 6 and 12 month post-operativelyForce applied by the tip of the thumb and the tip of the index finger, measured by a goniometer in kilograms
Change in functional performance as measured by Key Pinch Strength1 week pre-operatively and 3, 6 and 12 month post-operativelyForce applied by the pad of the thumb and lateral surface of the index finger, measured by a goniometer in kilograms

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026