Palmaris Longus Muscle and Dupuytren

NCT06281509 — Not applicable, Completed, 243 participants, Universitaire Ziekenhuizen KU Leuven

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The Potential Relationship Between the Palmaris Longus Muscle Prevalence and Dupuytren Disease: a Comparative Study

RegistryNCT06281509, acronym Palmaris
StatusCompleted
PhaseNot applicable
Study typeInterventional; non randomized, parallel, masking: none, diagnostic
Enrollment243 (Actual)
SponsorUniversitaire Ziekenhuizen KU Leuven (Other)
ConditionsDupuytren's Disease
InterventionsNon-invasive tests to determine the presence or absence of the palmaris longus tendon in both hands., Ultrasound (Procedure)
Datesstart 2024-02-16, primary completion 2025-11-28, completion 2025-11-28, first posted 2024-02-28, last updated 2026-03-09
Locations1 site in Belgium

Related Papers Related Patents Related Grants Related Experts
All trials for Dupuytren's Disease All trials of Non-invasive tests to determine the presence or absence of the palmaris longus tendon in both hands. All trials of Ultrasound

-Summary

Dupuytren disease is a medical condition characterized by the painless formation of nodules in the palm of the hand. Cords are formed on the palmar fascia, a connective tissue sheet in the palm of the hand. This fascia is seen as the vestigial remnant of the palmaris longus tendon. The PLM attaches to the fascia palmaris. A muscle that not everyone has and can therefore be clearly missed. This raises the question of whether the presence of the musculus palmaris longus has any association with the development, recurrence and/or progression of DD and contractures. To investigate a potential predisposition, this study intend to assess the prevalence of the PLM in a group of individuals affected by DD and compare it with a control group (age matched, no signs of DD) without the condition.

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+Detailed description

Dupuytren disease is also known as Dupuytren contracture. It is a medical condition characterized by the painless formation of nodules in the palm of the hand. As the disease progresses, approximately 21% - 50% of all patients experience a transformation of these nodules (stage 0/N of Tubiana) into cord-like structures. These cords, in turn, lead to finger contractures (Tubiana stages 1-4) with impairment of hand mobility and stiffening of the palmar skin. The cords are formed on the palmar fascia, a connective tissue sheet in the palm of the hand. This fascia is seen as the vestigial remnant of the palmaris longus tendon. The PLM attaches to the fascia palmaris. A muscle that not everyone has and can therefore be clearly missed. This raises the question of whether the presence of the musculus palmaris longus has any association with the development, recurrence and/or progression of DD and contractures. To investigate a potential predisposition, this study intend to assess the prevalence of the PLM in a group of individuals affected by DD and compare it with a control group (age matched, no signs of DD) without the condition. Interestingly, prior research has already explored this topic. Despite the publication dating back to 1986, it reported a significantly higher occurrence of the palmaris longus tendon in patients affected by DD. Furthermore, a second article from the same year concluded a significant decrease in recurrence when the palmaris longus tendon was resected in combination with regional fasciectomy. Remarkably, no other research on this topic was found despite the promising results of both articles.

+Arms and interventions

ArmTypeInterventionsDescription
Patients with Dupuytren diseaseExperimentalProcedure: Non-invasive tests to determine the presence or absence of the palmaris longus tendon in both hands.; Procedure: Ultrasound120 individuals diagnosed with Dupuytren disease (primary or recurrent).
Healthy controlsExperimentalProcedure: Non-invasive tests to determine the presence or absence of the palmaris longus tendon in both hands.; Procedure: Ultrasound120 participants with no other medical conditions affecting the function of the hand (musculoskeletal pathology, vascular or neurological conditions such as CRPS, rheumatoid arthritis and paralysis).
  • Non-invasive tests to determine the presence or absence of the palmaris longus tendon in both hands. (Procedure): Schaeffer's test (flexion of the wrist while the pinky and thumb are pressed against each other) Thompson's test (wrist flexion with a clenched fist) Mishra test I (wrist flexion while the examiner pushes the hand back) Mashra test II (thumb opposition while flexing the wrist)
  • Ultrasound (Procedure): A small mobile ultrasound device will be used to further asses the presence of the tendon.

+Outcome measures

Primary outcomes

  • PLM in the DD versus control [Baseline]: Percentual prevalence of the Palmaris Longus Muscle in the Dupuytren Disease-group versus the control group.
  • PML in mild versus severe DD-group [Baseline]: Percentual prevalence of the Palmaris Longus Muscle in the mild (stage 0/N of Tubiana) Dupuytren Disease-group versus the severe (Tubiana stages 1-4) Dupuytren Disease-group.

Secondary outcomes

  • PLM presence in DD affected group [Baseline]: Percentual prevalence of the Palmaris Longus Muscle in the Dupuytren Disease-group
  • PLM presence in control group [Baseline]: Percentual prevalence of the Palmaris Longus Muscle in the control group
  • Dominant versus non-dominant hand [Baseline]: Percentual prevalence of the Palmaris Longus Muscle in the dominant hand versus the non-dominant hand for both Dupuytren Disease-group and control group.
  • Male versus female population [Baseline]: Percentual prevalence of the Palmaris Longus Muscle in male versus female population.

+Eligibility

Sex: All, ages: 50 Years to any, accepts healthy volunteers

Inclusion Criteria:

* The participant or his/her legally authorized representative voluntary signed the informed consent prior to the first assessment.
* 50 years of age or higher.
* Has Dupuytren disease (primary or recurrent). (Only applicable for participants of DD group)
* Has no medical conditions affecting the function of the hand (musculoskeletal pathology, vascular or neurological conditions such as CRPS, rheumatoid arthritis and paralysis). (Only applicable for participants of control group)

Exclusion Criteria:

* Patients < 50 years
* Patients with cognitive impairments.
* Patients showing signs of medical conditions affecting the function of the hand (musculoskeletal pathology, vascular or neurological conditions such as CRPS, rheumatoid arthritis and paralysis). (Only applicable for participants of control group)

+Locations (1)

FacilityCityCountryStatus
Universitaire Ziekenhuizen KU LeuvenLeuven, Vlaams-BrabantBelgium

+Investigators