FLEX-Trial: Prospective Sonographic Assessment Of Healing Process

See also
Status	Clinical Trial	Phase
Completed	`NCT00537784` - Platelet Concentrate in Achilles Tendon Repair	N/A
Withdrawn	`NCT01497678` - Musculotendinous Tissue Unit Repair and Reinforcement (MTURR) Coordinating Center	N/A
Recruiting	`NCT01063465` - Measurement of Mechanical Properties of the Healing Achilles Tendon With or Without Early Weightbearing	N/A
Completed	`NCT01292876` - Musculotendinous Tissue Repair Unit and Reinforcement (MTURR)	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT00537784 - Platelet Concentrate in Achilles Tendon Repair

N/A

Withdrawn

NCT01497678 - Musculotendinous Tissue Unit Repair and Reinforcement (MTURR) Coordinating Center

N/A

Recruiting

NCT01063465 - Measurement of Mechanical Properties of the Healing Achilles Tendon With or Without Early Weightbearing

N/A

Completed

NCT01292876 - Musculotendinous Tissue Repair Unit and Reinforcement (MTURR)

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01013428
Study type	Observational
Source	University of Zurich
Contact
Status	Completed
Phase	N/A
Start date	November 2009
Completion date	January 2016

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms