FLEX-Trial: Prospective Sonographic Assessment Of Healing Process Following Suture of Profound Flexor Tendon Due to Traumatic Rupture of FDP-Tendon in Zone II.

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2010 by University of Zurich.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University of Zurich
ClinicalTrials.gov Identifier:
NCT01013428
First received: November 11, 2009
Last updated: June 24, 2010
Last verified: June 2010
  Purpose

To prospectively assess the healing process following suture of profound fexor tendon due to traumatic rupture of FDP-Tendon in Zone II by ultrasound.


Condition Intervention
Tendon Injury
Other: Ultrasound

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Further study details as provided by University of Zurich:

Estimated Enrollment: 50
Study Start Date: November 2009
Estimated Study Completion Date: December 2011
Intervention Details:
    Other: Ultrasound
    Ultrasound will be used to evaluate tendons.
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

primary care clinic

Criteria

Inclusion criteria:

  • All patients with traumatic rupture of FDP-tendon in zone II.

Exclusion criteria:

  • < 18years;
  • Fracture;
  • crush injury; (partial) amputation;
  • RA;
  • CPPD;
  • CP;
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01013428

Contacts
Contact: 01 Studienregister MasterAdmins +41 (0)44 255 11 11

Locations
Switzerland
Recruiting
Zurich, Switzerland
Sponsors and Collaborators
University of Zurich
Investigators
Study Director: 01 Studienregister MasterAdmins UniversitaetsSpital Zuerich
  More Information

No publications provided

Responsible Party: Andreisek G, MD, University Hospital Zürich
ClinicalTrials.gov Identifier: NCT01013428     History of Changes
Other Study ID Numbers: 001
Study First Received: November 11, 2009
Last Updated: June 24, 2010
Health Authority: Switzerland: Swissmedic

Keywords provided by University of Zurich:
Traumatic Rupture of Tendon

Additional relevant MeSH terms:
Tendon Injuries
Wounds and Injuries

ClinicalTrials.gov processed this record on July 20, 2014