Percutaneous Aponeurotomy in the Treatment of Dupuytren's Disease

NCT ID: NCT02474576

Last Updated: 2021-02-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

130 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-30

Study Completion Date

2020-04-30

Brief Summary

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The efficiency of percutaneous aponeurotomy in the treatment of Dupuytrens disease is well known. However, the duration of the clinical improvement after aponeurotomy is not well known.

This study aims primarily at measuring the incidence rate of local relapse of Dupuytrens-induced finger flessum, within two years following treatment by percutaneous aponeurotomy in Dupuytrens.

Detailed Description

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Conditions

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Dupuytren Disease

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Percutaneous aponeurotomy

Treatment of Dupuytrens-induced finger flessum using percutaneous aponeurotomy

Group Type EXPERIMENTAL

Percutaneous aponeurotomy

Intervention Type PROCEDURE

The finger(s) with limited extension due to Dupuytrens disease and for which the patient desires treatment, will be treated by fine-needle percutaneous aponeurotomy under local anesthesia (outpatient procedure). This procedure is already routinely used in clinical practice ; our study aims at better describing the time-sustainability of its benefits.

Interventions

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Percutaneous aponeurotomy

The finger(s) with limited extension due to Dupuytrens disease and for which the patient desires treatment, will be treated by fine-needle percutaneous aponeurotomy under local anesthesia (outpatient procedure). This procedure is already routinely used in clinical practice ; our study aims at better describing the time-sustainability of its benefits.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient suffers from Dupuytren disease
* Patient has at least one finger with at least 20° flessum on the metacarpophalangeal joint and/or on the proximal interphalangeal joint
* Patient has chosen to benefit from local treatment

Exclusion Criteria

* Pregnancy
* Breastfeeding
* No social insurance
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Groupe Hospitalier Diaconesses Croix Saint-Simon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Diaconesses Croix Saint-Simon Hospital Group

Paris, , France

Site Status

Countries

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France

Other Identifiers

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MMN_2015-1

Identifier Type: -

Identifier Source: org_study_id

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