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Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

This study has been withdrawn prior to enrollment.
(Study has never started)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00285987
First Posted: February 2, 2006
Last Update Posted: December 28, 2007
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:
University Hospital, Ghent
  Purpose
Study to compare the quality of life after reconstruction of the cruciate ligament in hospitalized versus day-clinic patient

Condition Intervention
Rupture of the Cruciate Ligament Procedure: Reconstruction of the cruciate ligament

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

Resource links provided by NLM:


Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Quality of life

Estimated Enrollment: 500
  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 to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • rupture of the cruciate ligament

Exclusion Criteria:

  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): NCT00285987


Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Rene Verdonk, MD, PhD University Hospital, Ghent
  More Information

Additional Information:
ClinicalTrials.gov Identifier: NCT00285987     History of Changes
Other Study ID Numbers: 2000/282
First Submitted: February 1, 2006
First Posted: February 2, 2006
Last Update Posted: December 28, 2007
Last Verified: December 2007

Additional relevant MeSH terms:
Rupture
Wounds and Injuries