Zurich, Switzerland
NCT Number: NCT01013428
FLEX-Trial: Prospective Sonographic Assessment Of Healing Process Following Suture of Profound Flexor Tendon Due to Traumatic Rupture of FDP-Tendon in Zone II.
To prospectively assess the healing process following suture of profound fexor tendon due to traumatic rupture of FDP-Tendon in Zone II by ultrasound.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- All patients with traumatic rupture of FDP-tendon in zone II.
Exclusion criteria
- < 18years;
- Fracture;
- crush injury; (partial) amputation;
- RA;
- CPPD;
- CP;
Treatment and study plan
ultrasound
OtherUltrasound will be used to evaluate tendons.
Sponsors and collaborators
Lead sponsor
University of Zurich
Other
Registry information
Important dates
- Study start
- 2009
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Nov 13, 2009
- Registry last updated
- Mar 30, 2016
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.
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