Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

This study has been withdrawn prior to enrollment.

(Study has never started)

Sponsor:

Information provided by:

University Hospital, Ghent

ClinicalTrials.gov Identifier:

NCT00285987

First received: February 1, 2006

Last updated: December 19, 2007

Last verified: December 2007

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 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:

MedlinePlus related topics: Plastic and Cosmetic Surgery

U.S. FDA Resources

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

Additional Information:

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

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:

Rupture
Wounds and Injuries

ClinicalTrials.gov processed this record on May 19, 2013