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OpenTrials
Completed

NCT Number: NCT04607187

Ultrasound B Mode Imaging and Elastography

A Pilot Study on Ultrasound B mode Imaging and Elastography during administration of Xiaflex (collagenase clostridium histolyticum) for Dupuytren's contracture.

Completed

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Key information

Conditions

Dupuytren's Contractures

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The Center for Rheumatology and Bone Research a division of Arthritis and Rheumatism Associates, P.C.

Wheaton, Maryland, 20902, United States

About this study

Ultrasound analysis will be obtained on patient that receives Xiaflex as standard of care for Dupuytren's contracture

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Normal Hand or Hand Dupuytren's contracture

Exclusion criteria

  • Previous treatment of Dupuytren's cord

Treatment and study plan

Primary outcomes

  1. Ultrasound B mode Imaging and Elastography

    Time frame: 30 day trial

    A Pilot Study: Ultrasound B mode Imaging and Elastography during administration of Xiaflex

Sponsors and collaborators

Lead sponsor

Theresa Bass-Goldman

Other

Collaborators

  • Endo USA Inc., a Keenova Therapeutics Company

Registry information

Official study title

Ultrasound B Mode Imaging and Elastography During Administration of Xiaflex (Collagenase Clostridium Histolyticum) for Dupuytren's Contracture: A Pilot Study (The UBIEX-DC Study)

Acronym: UBIEX-DC

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Oct 29, 2020
Registry last updated
Oct 29, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.