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Cost Efficacy of a Clinical Pathway to Patients Undergoing Hip and Knee Replacement Surgery

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2006 by University of Aarhus.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT00175201
First received: September 10, 2005
Last updated: May 4, 2006
Last verified: May 2006
  Purpose

In this randomised study a proactive care and rehabilitation intervention is compared to the current care and rehabilitation in patients undergoing primary hip and knee replacement surgery.

A cost efficacy analysis in a societal perspective is made from effect data in the randomised controlled study together with cost data gathered during the perioperative and postoperative period.

If the proactive care and rehabilitation intervention is cost effective the intervention is going to be implemented in Ringkøbing County. This implementation proces is measured within a monitoring project of all patients receiving hip or knee replacement surgery in Ringkøbing County in the period 2003 to 2007.


Condition Intervention
Osteoarthritis
Procedure: Proactive care and rehabilitation

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: From Efficacy to Effectiveness of a Proactive Perioperative Care and Rehabilitation in Patients Undergoing Primary Total Hip or Knee Replacement

Resource links provided by NLM:


Further study details as provided by University of Aarhus:

Primary Outcome Measures:
  • Health relatede quality of life
  • Pain
  • Disabillity
  • Costs

Estimated Enrollment: 80
Study Start Date: May 2005
Estimated Study Completion Date: March 2008
  Show Detailed Description

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Primary osteoarthritis of the hip and knee -

Exclusion Criteria:

Non-cooperative Replacement secondary to fracture Revision surgery

-

  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00175201

Contacts
Contact: Kristian Larsen

Locations
Denmark
Kristian Larsen Recruiting
Holstebro, Jutland, Denmark, 7500
Contact: Kristian Larsen, MPH    +45 25387052    fekl@larsen.tdcadsl.dk   
Principal Investigator: Kristian Larsen, MPH         
Sponsors and Collaborators
University of Aarhus
Investigators
Study Chair: Kjeld Søballe, DMSC Orthopaedic Center, Aarhus University Hospital, Aarhus, Denmark
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00175201     History of Changes
Other Study ID Numbers: KL-05-01
Study First Received: September 10, 2005
Last Updated: May 4, 2006
Health Authority: Denmark: The Danish National Committee on Biomedical Research Ethics

Additional relevant MeSH terms:
Osteoarthritis
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases

ClinicalTrials.gov processed this record on November 20, 2014