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Hand Ligament Reconstructions With Knee Collateral Ligament Allografts

Hand Ligament Reconstructions With Knee Collateral Ligament Allografts

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05060900
Enrollment
45
Registered
2021-09-29
Start date
2021-09-30
Completion date
2023-09-30
Last updated
2021-09-29

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

Conditions

Hand Injuries, Ligament Avulsion, Ligament Injury, Ligament Rupture, Wrist Injuries

Keywords

hand ligament injury, wrist ligament injury

Brief summary

The purpose of this study is to review the clinical outcomes following hand ligament reconstruction surgery using allograft (cadaveric) knee collateral ligaments. Currently, there is no standard procedure or devices used for hand ligament reconstruction surgery, although most techniques use some form of autograft (patients' own tissue) for the reconstruction. We believe that the use of allograft ligaments in reconstruction may eliminate the pain associated with procuring the patients' own tissue for the procedure, and prove to be a viable and preferred alternative to the multiple techniques currently used. The main procedures of this study include wrist and hand ligament reconstruction surgery (for wrist scapholunate (SL) ligaments, thumb ulnar collateral ligaments (UCL), and finger proximal interphalangeal (PIP) joint collateral ligaments) using allograft ligament, and subsequent follow up appointments where measurements and questionnaires will be completed to evaluate how hand function is doing after surgery.

Interventions

PROCEDURELigament Reconstruction with Allograft Ligament

Patients will undergo surgery for hand and wrist ligament reconstruction using allograft ligament.

Sponsors

Cedars-Sinai Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

All patients enrolled in the study will undergoing their ligament reconstruction procedure with allograft ligament.

Eligibility

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

Inclusion criteria

* Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Have symptomatic injuries to either their finger PIP collateral ligaments, thumb UCL ligaments, or wrist SL ligaments and have failed non-operative management for the above ligament injuries (thus eligible for operative reconstruction) * Age over 18 years

Exclusion criteria

* Presence of any other current injury in that limb * Presence of advanced arthrosis in that limb * Presence of fixed joint deformity in that limb * Presence of instability in that limb due to bony or articular instability * Presence of instability in that limb due to inflammatory arthrosis * Is under 18 years of age * Lacks the capacity to consent

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in functional outcome, as measured by the quick Disabilities of the Arm, Shoulder and Hand (qDASH) questionnaireBaseline, post-surgery 6 week, post-surgery 6 month, post-surgery 1 yearThe qDASH questionnaire asks about symptoms of upper extremity disability as well as the ability to perform certain activities. It generates a score from 0 to 100, with higher scores indicating greater severity of disability.
Change from baseline in pain, as measured by the Visual Analog Scale (VAS)Baseline, post-surgery 6 week, post-surgery 6 month, post-surgery 1 yearThe VAS generates a scale from 0 to 100 with 0 indicating no pain and higher scores indicating greater pain.
Change from baseline in key pinch strength, as measured with a pinch gauge.Baseline, post-surgery 6 week, post-surgery 6 month, post-surgery 1 yearA pinch gauge is a device that measures key pinch strength in units of pounds or Newtons.
Change from baseline in grip strength, as measured with a Jamar hand dynamometer.Baseline, post-surgery 6 week, post-surgery 6 month, post-surgery 1 yearA Jamar hand dynamometer is a device that measures grip strength in units of pounds or Newtons.
Change from baseline in wrist and finger range of motion angles.Baseline, post-surgery 6 week, post-surgery 6 month, post-surgery 1 yearRange of motion to be assessed includes wrist extension, wrist flexion, wrist ulnar deviation, wrist radial deviation, finger proximal interphalangeal joint flexion and extension, thumb metacarpophalangeal joint flexion and extension, thumb abduction and adduction.
Change from baseline in wrist and finger radiographs.Baseline, post-surgery 6 week, post-surgery 6 month, post-surgery 1 yearRadiographic images obtained can help indicate the success of surgery by demonstrating joint stability.

Countries

United States

Contacts

Primary ContactMichael Sun, MD
michael.sun@cshs.org858-414-8733

Outcome results

None listed

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