Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

This study has been withdrawn prior to enrollment.
(Study has never started)
Information provided by:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
First received: February 1, 2006
Last updated: December 19, 2007
Last verified: December 2007

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
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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

Ages Eligible for Study:   18 Years to 50 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • rupture of the cruciate ligament

Exclusion Criteria:


  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00285987

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

Additional Information:
No publications provided

ClinicalTrials.gov Identifier: NCT00285987     History of Changes
Other Study ID Numbers: 2000/282
Study First Received: February 1, 2006
Last Updated: December 19, 2007
Health Authority: Belgium: Institutional Review Board

Additional relevant MeSH terms:
Wounds and Injuries

ClinicalTrials.gov processed this record on April 16, 2014