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

Tendon Injury Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01013428
• Other study ID #: 001
• Status: Completed
• Phase: N/A
• First received: November 11, 2009
• Last updated: March 29, 2016
• Start date: November 2009
• Est. completion date: January 2016

Study information

• Verified date: March 2016
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Health authority: Switzerland: Swissmedic
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: January 2016
• Est. primary completion date: January 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion criteria:

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

Exclusion criteria:

• < 18years;

• Fracture;

• crush injury; (partial) amputation;

• RA;

• CPPD;

• CP;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Tendon Injuries
• Tendon Injury

Intervention

Other:
• Ultrasound
Ultrasound will be used to evaluate tendons.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland,