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Diagnostic Accuracy of Direct MR Arthrography Of The Wrist At 1.5, 3.0 And 7.0T

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01012271
First Posted: November 13, 2009
Last Update Posted: March 30, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Gustav Andreisek, University of Zurich
  Purpose
The purpose of our study is to evaluate the diagnostic accuracy of MR arthrography of the wrist at 1.5, 3.0, and 7.0T with wrist arthroscopy as reference standard.

Condition Intervention
Wrist Injuries Other: MRI

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Gustav Andreisek, University of Zurich:

Enrollment: 70
Study Start Date: October 2010
Study Completion Date: January 2016
Primary Completion Date: January 2016 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: MRI
    MR arthrography is used to evaluate wrist abnormalities
  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
primary care clinic
Criteria

Inclusion criteria:

  • age >18;
  • clinical evidence for wrist joint abnormalities;
  • request for MR arthrography prior to wrist arthroscopy;
  • willingness to take part in our study with written informed consent;

Exclusion criteria:

  • age<18;
  • history of prior wrist surgery; systemic diseases e.g. rheumatoid arthritis;
  • infection; history of adverse contrast reactions;
  • contraindication for MR imaging (e.g. pacemaker, metallic implants, etc.);
  • history or possible signs of renal failure (see section "nephrogenic systemic fibrosis")
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01012271


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

Responsible Party: Gustav Andreisek, mg, University of Zurich
ClinicalTrials.gov Identifier: NCT01012271     History of Changes
Other Study ID Numbers: 002
First Submitted: November 11, 2009
First Posted: November 13, 2009
Last Update Posted: March 30, 2016
Last Verified: March 2016

Keywords provided by Gustav Andreisek, University of Zurich:
Wrist abnormalities

Additional relevant MeSH terms:
Wrist Injuries
Arm Injuries
Wounds and Injuries