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CompletedNCT07082075Updated Jul 24, 2025

Joint Hyperlaxity and Volar Plate Dynamics: MRI-Based Comparative Evaluation of the PIP Joint

An observational study in Hypermobility, Joint, sponsored by Hacettepe University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-24.

Sponsored by Hacettepe University · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
32
Ages
18 Years to 65 Years
Sex
All
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Study summary

Background: The volar plate (VP) is a key stabilizer of the proximal interphalangeal joint (PIPJ), and its biomechanical behavior may be altered in individuals with joint hypermobility.

Objective: This study aimed to evaluate the spatial dynamics of the VP and its relationship with the center of joint motion and flexor digitorum profundus (FDP) tendon in individuals with and without joint hyperlaxity using MRI.

Methods: Thirty-two healthy volunteers (16 hyperlax, 16 controls) underwent MRI imaging of both index fingers at five flexion angles (0°, 30°, 60°, 90°, full flexion) and under passive and isometric loading conditions. Key parameters measured included distances from the joint center to VP attachments, VP-FDP tendon distance, and the length between VP ends.

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Conditions studied

  • Hypermobility, Joint

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Keywords

  • volar plate
  • hypermobility
  • biomechanics
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In context

Joint Instability

115 studies on the registry are indexed under Joint Instability; 21 are open to participants now.

This study's enrollment of 32 is below the median of 60 across 54 observational studies indexed under Joint Instability.

Browse Joint Instability studies →

Lead sponsor

Hacettepe University is the lead sponsor of 1,007 studies on the registry; 214 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Healthy and hypermobility volunteers

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • between 18-65 years

Exclusion criteria

Exclusion Criteria:

  • any history of acute or overuse injuries to the examined hand,
  • any prior surgical procedures on the examined upper extremity.
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
32 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. The Distance Between the Center of Motion (CoM) and the VPLip and VPTip

    The distances between the center of motion (CoM) and the volar lip of the middle phalanx base (VPLip), and between the CoM and the proximal end of the volar plate at its attachment to the volar base of the proximal phalanx (VPTip), were measured using RadiAnt DICOM Viewer software (version 2024.1) in various PIPJ angles.

    Time frame: baseline

  2. The Distance Between VPLip and VPTip

    The distance between the volar lip of the middle phalanx base (VPLip), and the proximal end of the volar plate at its attachment to the volar base of the proximal phalanx (VPTip) measured using RadiAnt DICOM Viewer software (version 2024.1) in various PIPJ angles. The purpose of this measurement was to observe how the distance between the two ends of the volar plate changes with varying joint angles.

    Time frame: baseline

  3. The Distance Between Volar Plate (VP) and FDP Tendon

    The distance between the midpoint of the volar plate (VP) and the flexor digitorum profundus (FDP) tendon was measured using RadiAnt DICOM Viewer software (version 2024.1) at various proximal interphalangeal joint (PIPJ) angles. The purpose of this measurement was to observe how this distance changes across different flexion angles.

    Time frame: baseline

  4. Changes Observed During Grasping and Isometric Contraction

    Measurements at all flexion angles were conducted under two conditions: while passively grasping a cylindrical object (without force) and during isometric contraction (with force).

    Time frame: baseline

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Study locations

1 site
  • Hacettepe University
    Ankara, Ankara 06100, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: Undecided — It can not be ethical.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07082075
Collaborators
Baskent University Ankara Hospital
Responsible party
Cigdem Ayhan (Professor, Hacettepe University) — Principal investigator
First posted
Jul 24, 2025
Start date
May 15, 2023
Primary completion
Jul 15, 2023
Completion
May 15, 2024
Last update
Jul 24, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2025. You cannot join it, but the record below documents what was studied.

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