Recruiting

Thumb Strength

Sponsor:

Dartmouth-Hitchcock Medical Center

Code:

NCT04458584

Conditions

Osteoarthritis Thumb

Eligibility Criteria

Sex: All

Age: 21+

Healthy Volunteers: Not accepted

Interventions

Trapeziectomy with ligament reconstruction (I; LRTI)

Trapeziectomy with suture suspensionplasty (II; SS)

Arthroscopic Trapeziectomy (III; AT)

Study Details

Brief summary:

The purpose of this study is to evaluate the basis for three widely held fundamental tenets about surgical intervention for thumb basal joint arthritis;

1. Trapeziectomy with ligament reconstruction and metacarpal stabilization is associated with superior functional outcomes and strength,
2. Preservation of the arthroplasty space correlates with functional outcomes, pain relief, and restoration of strength after basal joint arthroplasty, and
3. Mitigation of metacarpophalangeal joint (MCPJ) hyperextension optimizes postoperative strength after basal joint arthroplasty, regardless of surgical technique.

It is hypothesized that thumb basal joint arthroplasty with metacarpal stabilization, by either ligament reconstruction (I) or suture suspension (II), provides greater improvement in grip and pinch strength, and better hand function, than might be achieved following provision of pain relief alone by simple trapeziectomy (III). Preservation of the arthroplasty space will correlate positively, and MCPJ hyperextension will correlate negatively, with improved thumb function and lateral pinch strength.

Primary Aims (within 3 procedure cohorts):

1. Compare pre-operative pinch and grip strength as well as patient-reported outcomes (PROs) for pain in patients before and after lidocaine injection of the trapeziometacarpal joint, prior to thumb basal joint arthroplasty;
2. Compare post-operative pinch and grip strength and PROs for pain and function at 3 and 6 months after thumb basal joint arthroplasty with pre-operative values before and after lidocaine injection;
3. Correlate preservation of dynamic arthroplasty space as measured on a stress radiograph with postoperative improvement in pinch and grip strength, and PROs for pain and function;
4. Correlate dynamic MCP joint position and laxity with change in strength and patient-reported pain and function to define optimal MCPJ position.

Secondary Aims (between 3 procedure cohorts):

1. Compare change in pre- and post-operative pinch and grip strength and PROs for pain and function between patients having basal joint arthroplasty with and without specific metacarpal stabilization;
2. Compare preservation of the dynamic arthroplasty space and improvement in strength and patient-reported pain and function between arthroplasty groups; and
3. Compare changes in pinch and grip strength and PROs for pain and function with dynamic MCPJ position between arthroplasty groups.
4. Compare postoperative neuritis and complications between surgical groups.

Conditions

Osteoarthritis Thumb

Study ID

NCT04458584

Start date

Jun 29, 2020

Status verified date

Jul, 2026

Completion date

Mar 31, 2027

Anticipated

Primary completion date

Dec 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 21+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Males and females 21 years of age or older;
  • Undergoing elective non-prosthetic, primary basal joint arthroplasty;
  • Patient has necessary mental capacity to participate and comply with study protocol;
  • Patient is willing and able to give informed consent; and
  • Patient is willing to participate under the care of their chosen surgeon.

Exclusion Criteria:

  • Patients with a diagnosis of rheumatoid arthritis, systemic lupus erythematosis, psoriatic arthritis, or other related inflammatory arthritis;
  • Patients undergoing simultaneous bilateral hand procedures of any nature;
  • Women who are pregnant or breastfeeding;
  • Women of reproductive potential unless there is a negative urine pregnancy test on the day of surgery. Women of child bearing potential include those who are premenopausal who have not had a bilateral oophorectomy, hysterectomy or tubal ligation. Post-menopausal is defined as not having had a menstrual period for at least one calendar year.
  • Vulnerable patient populations including prisoners and institutionalized individuals.

Study Design

Enrollment

165 participants

Anticipated

Interventions and Outcome Measures

Arms

Ligament Reconstruction - Tendon Interposition (LRTI)

Patients undergoing thumb basal joint arthroplasty using LRTI procedure as treatment of osteoarthritis.

Suture Suspensionplasty (SS)

Patients undergoing thumb basal joint arthroplasty using suture suspensionplasty (SS) procedure as treatment of osteoarthritis.

Arthroscopic Trapeziectomy (AT)

Patients undergoing thumb basal joint arthroplasty using arthroscopic trapeziectomy (AT) procedure as treatment of osteoarthritis.

Interventions

Trapeziectomy with ligament reconstruction (I; LRTI)

Thumb basal joint arthroplasty (surgical) using Trapeziectomy with ligament reconstruction (I; LRTI)

Trapeziectomy with suture suspensionplasty (II; SS)

Thumb basal joint arthroplasty (surgical) using Trapeziectomy with suture suspension-lastly (II; SS)

Arthroscopic Trapeziectomy (III; AT)

Thumb basal joint arthroplasty (surgical) using Arthroscopic Trapeziectomy (III; AT)

Primary outcome measure

  • Change in pre-operative pinch and grip strength as measured by kilograms of pressure within and between procedure cohorts before and after lidocaine injection of the trapeziometacarpal joint. [ Time Frame: Preoperative baseline, both before and after basal joint lidocaine injection, and then 3 months and 6 months after surgery ]
  • Change in Pain, pre- to post-operatively, as measured by a standard visual analogue score (VAS) diagram to grade perceived pain within and between procedure cohorts. [ Time Frame: Preoperative baseline, both before and after basal joint lidocaine injection, and then 3 months and 6 months after surgery ]
  • Change in Patient-Reported Function as measured by the short form Disabilities of the Arm, Shoulder, and Hand (QuickDASH) questionnaire, within and between procedure cohorts. [ Time Frame: Baseline, 3 months and 6 months after surgery ]
  • Change in Quality of Life as measured by the PROMIS-10 Global Health questionnaire, within and between procedure cohorts. [ Time Frame: Baseline, 3 months and 6 months after surgery ]

Central Contacts and Locations

Central contacts

Locations

Dartmouth-Hitchcock Medical Center

Recruiting

Lebanon, New Hampshire, United States, 03756

Contacts

More Information

Sponsor

Dartmouth-Hitchcock Medical Center

Last update posted

Jul 30, 2026

Last verified

Jul, 2026

Keywords

  • Ligament reconstruction
  • Suspensionplasty
  • Arthroscopic Trapeziectomy

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Dartmouth-Hitchcock Medical Center on 2026-07-30.