- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05835830
Thumb Metacarpophalangeal Hyperextension in an Arthritic Population; Part 2
Study Overview
Status
Conditions
Detailed Description
To date, no studies have looked at the relationship of preoperative and postoperative MP pinch position and passive MP hyperextension in an arthritic patient population. Other research has found that dynamic thumb MP pinch position is independent of passive MP hyperextension in a healthy non-arthritic population (thumbs with passive MP hyperextension on exam did not pinch in a position of MP hyperextension), but no such investigation has been performed in an arthritic population pre and postoperatively. It is also undetermined which of these parameters (dynamic pinch or passive MP hyperextension) has a larger correlation to postoperative outcomes following basilar joint arthroplasty, and which parameter should be considered when determining whether or not to surgically stabilize the MP joint at the time of CMC arthroplasty.
The specific aim of this study is to compare the preoperative and postoperative changes in dynamic and passive range of motion of the thumb MP joint in patients undergoing CMC basilar joint reconstruction without concomitant MP joint stabilization.
Secondary aims of this study will be to compare postoperative pinch and grasp strength, radiographic subsidence and longitudinal collapse, in addition to postoperative patient reported outcomes in patients with good dynamic MP control (<5 degrees) vs poor dynamic control (>5degrees)
The hypothesis is that dynamic thumb MP pinch position will not change compared with its preoperative status. Investigators also hypothesize that patients with better dynamic pinch position postoperatively will have better pinch strength and better functional outcomes than patients with poor dynamic pinch position.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
Indiana
-
Indianapolis, Indiana, United States, 46260
- Indiana Hand to Shoulder Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
• Adults (18 years of age or older)
- Patients presenting with symptomatic 1st CMC arthritis with or without scaphotrapeziotrapezoid arthritis
- Eaton Classification stage II, III, or IV OA of the first CMC joint based on xrays
- Patients who plan to undergo a ligament reconstruction and tendon interposition (LRTI) or thumb suspensionplasty procedure within 6 months of enrolling to study
Patients with greater than 20 degrees of passive MP Hyperextension
o Screened by surgeons upon first evaluation in clinic
- Bilateral thumbs included
Exclusion Criteria:
• <18 years age
- Prior surgical history of ipsilateral 1st CMC arthroplasty or procedures involving thumb MP or CMC joints
- Prior ipsilateral 1st ray deformity or malunion, distal radial malunion or nonunion, 2nd ray amputation or deformity
- Prior ipsilateral tendon rupture or ipsilateral peripheral nerve palsy
- Inflammatory arthritis
- Post-traumatic CMC arthritis
- Prior trauma to the MP or CMC joints
- Diagnosis of Ehler-Danlos syndrome or other connective tissue disorder
- Concomitant treatment of the MP joint
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Passive Thumb MP Hyperextension
Time Frame: 12 months
|
degree of MP Hyperextension measured in clinic
|
12 months
|
|
Dynamic thumb MP Hyperextension (key pinch)
Time Frame: 12 months
|
lateral key pinch measured with pinch gauge
|
12 months
|
|
Dynamic thumb MP position during cylindrical grasp
Time Frame: 12 months
|
range of motion measure of thumb MP joint around a cylindrical object (peanut butter jar and water bottle)
|
12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MP Hyperextension
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on CMC Arthritis
-
University of CalgaryNot yet recruiting
-
Loci OrthopaedicsRecruiting
-
Julie NuelleArthrex, Inc.RecruitingOccupational Therapy | Hand Arthritis | CMC ArthritisUnited States
-
Foundation for Orthopaedic Research and EducationRecruitingCarpometacarpal (CMC) Joint ArthritisUnited States
-
University of FloridaWithdrawnCarpometacarpal (CMC) Joint ArthritisUnited States
-
Karolinska InstitutetRecruitingOsteoarthritis of the CMC-1 JointSweden
-
Uppsala UniversityÖrebro County Council; Uppsala County Council, SwedenNot yet recruitingThumb Osteoarthritis | Thumb Carpometacarpal Joint Osteoarthritis | Basal Thumb Osteoartrithis | Carpometacarpal (CMC) Joint ArthritisSweden
-
Marie BadalamenteRecruitingCarpometacarpal (CMC) OsteoarthritisUnited States
-
Karolinska InstitutetErasmus Medical CenterCompletedOsteoarthritis in the Carpometacarpal (CMC) Joint
-
Herlev and Gentofte HospitalRecruitingTrapeziometacarpal Osteoarthritis | CMC-1 OsteoarthritisDenmark