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Prospective Randomized Trial Between Needle Fasciotomy and Xiapex for Dupuytrens Contracture

NCT02476461 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2015-06-19

No results posted yet for this study

Summary

The purpose of this study is to investigate whether percutaneous needle fasciotomy is as effective for treating Dupuytrens contracture as Xiapex. Immidiate treatment effect is to be investigated, as iskontracture size after 5 years. Contracture size after one and three years, and subjective hand function is also to be investigated.

Conditions

  • Dupuytrens Contracture

Interventions

DRUG

xiapex

PROCEDURE

percutaneous needle fasciotomy

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • hallgeir bratberg, MD · Oslo University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2016-04-30
Completion
2021-01-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02476461 on ClinicalTrials.gov