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Comparison of Dynamic Distraction Systems in Proximal Interphalangeal Joint Fractures

Comparison of Dynamic Distraction Systems in Proximal Interphalangeal Joint Fractures

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04470349
Acronym
DYNAFIX
Enrollment
30
Registered
2020-07-14
Start date
2020-07-14
Completion date
2024-06-30
Last updated
2023-01-26

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

Conditions

Proximal Interphalangeal Joint Fracture of the Hand

Brief summary

Fractures of the proximal interphalangeal joints continue to pose significant management challenges. Thus the aim of our study is to compare two dynamic finger joint distractors (Litos® and Ligamentotaxor®) in respect to the radiological standard follow-up examination and functional assessments.

Interventions

DEVICELITOS

Patients who received a LITOS dynamic distraction system after 31.12.2017

DEVICELigamentotaxor

Patients who received a Ligamentotaxor dynamic distraction system after 31.12.2017

Sponsors

Waldfriede Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* proximal interphalangeal fracture treated with external dynamic fixator * Operative care \<21 days from trauma * Age between 18 and 90 years. * Male and female

Exclusion criteria

\- additional fractures or disabilities of the hand

Design outcomes

Primary

MeasureTime frameDescription
Disabilities of Arm, Shoulder and Hand (DASH) score3 months after explantationDisabilities as measured by the DASH scale; No Difficulty (1), Mild Difficulty (2), Moderate Difficulty (3), Severe Difficulty (4), Unable (5)

Secondary

MeasureTime frameDescription
Visual analogue scale (VAS) pain3 months after explantationFrom 0mm (no pain) to 100mm (maximum pain imaginable)
Functional assessment: Goniometry3 months after explantationROM of each joint of the injured fingert with a goniometer.

Countries

Germany

Contacts

Primary ContactMarkus Bock, MD
m.bock@waldfriede.de00493081810201
Backup ContactMatthias Url, MD
m.url@waldfriede.de00493081810201

Outcome results

None listed

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