Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament - Tabular View

This Tabular View shows the required WHO registration data elements as marked by ^†

Tracking Information

First Received Date ^†

February 1, 2006

Last Updated Date

December 19, 2007

Start Date ^†

Current Primary Outcome Measures ^†

Quality of life

Original Primary Outcome Measures ^†

Same as current

Change History

Complete list of historical versions of study NCT00285987 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^†

Original Secondary Outcome Measures ^†

Descriptive Information

Brief Title ^†

Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

Official Title ^†

Quality of Life After an Ambulatory Reconstruction of the Cruciate Ligament

Brief Summary

Study to compare the quality of life after reconstruction of the cruciate ligament in hospitalized versus day-clinic patient

Detailed Description

Study Phase

Study Type ^†

Interventional

Study Design ^†

Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study

Condition ^†

Rupture of the Cruciate Ligament

Intervention ^†

Procedure: Reconstruction of the cruciate ligament

Study Arms / Comparison Groups

Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status ^†

Withdrawn

Enrollment ^†

500

Completion Date

Primary Completion Date

Eligibility Criteria ^†

Inclusion Criteria:

rupture of the cruciate ligament

Exclusion Criteria:

Gender

Both

Ages

18 Years to 50 Years

Accepts Healthy Volunteers

Contacts ^††

Location Countries ^†

Expanded Access Status

Administrative Information

NCT ID ^†

NCT00285987

Responsible Party

Secondary IDs ^††

Study Sponsor ^†

University Hospital, Ghent

Collaborators ^††

Investigators ^†

Principal Investigator:

Rene Verdonk, MD, PhD

University Hospital, Ghent

Information Provided By

University Hospital, Ghent

Verification Date

December 2007

^† Required WHO trial registration data element.
^†† WHO trial registration data element that is required only if it exists.