Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

This study has been withdrawn prior to recruitment.

Sponsored by:	University Hospital, Ghent
Information provided by:	University Hospital, Ghent
ClinicalTrials.gov Identifier:	NCT00285987

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:	Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study
Official Title:	Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:

Estimated Enrollment:

500

Eligibility

Criteria

Inclusion Criteria:

Exclusion Criteria:

Contacts and Locations

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

Sponsors and Collaborators

University Hospital, Ghent

Investigators

Principal Investigator:

Rene Verdonk, MD, PhD

University Hospital, Ghent

More Information

Website University Hospital Ghent This link exits the ClinicalTrials.gov site

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

Study placed in the following topic categories:

Quality of Life
Rupture

ClinicalTrials.gov processed this record on January 16, 2009