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Effects of Nerve Block on Knee Function After Knee Replacement

This study is currently recruiting participants.
Verified by Johns Hopkins University, July 2006

Sponsored by: Johns Hopkins University
Information provided by: Johns Hopkins University
ClinicalTrials.gov Identifier: NCT00358241
  Purpose

Early physical therapy after knee surgery is very painful on top of pain from surgery. Pain following surgery can limit recovery. One way to treat pain is by giving intravenous (IV) pain medication with morphine. Another method is to use a “nerve block” which involves placing a thin catheter (tube) into the lower back near the nerves that sense pain in the knee and give a local anesthetic to numb the nerves. Sometimes both methods are used together. This research is being done to determine whether nerve blocks with a local anesthetic improve knee recovery in addition to providing pain relief as compared to IV pain medicine alone


Condition Intervention
Postoperative Pain
Procedure: Nerve block

MedlinePlus related topics:   Knee Replacement   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Randomized, Double-Blind, Placebo Control, Parallel Assignment
Official Title:   Effects of Continuous Lumbar Plexus Nerve Block on Functional Restoration and Outcome After Unilateral Total Knee Arthroplasty
  Eligibility
Ages Eligible for Study:   21 Years to 80 Years
Genders Eligible for Study:   Both

Criteria

Inclusion Criteria:

  • Age 21-80 year old
  • ASA Physical Status ASA I and II
  • Mentally competent
  • Intellectually competent
  • Body mass index <35
  • No severe cardiac diseases
  • No severe pulmonary diseases
  • Unilateral knee disease
  • No other lower extremity joint disease
  • No chronic narcotic therapy or illicit drug use

Exclusion Criteria:

  • Age <21 or >80 year old
  • ASA Physical Status >ASA II
  • Mentally incompetent
  • Intellectually incompetent or cognitively impaired
  • Non-English speaking patient
  • Worker’s compensation patient
  • Body mass index > 35
  • Bilateral knee disease
  • Has other lower extremity joint disease
  • Severe cardiac diseases
  • Severe pulmonary diseases
  • Chronic narcotic therapy or illicit drug use
  • Pregnancy
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00358241

Contacts
Contact: A. Rollingson     410-550-0942    

Locations
United States, Maryland
Johns Hopkins Bayview Medical Center     Recruiting
      Baltimore, Maryland, United States, 21224
      Contact: A Rollingson     410-550-0942        

Sponsors and Collaborators
Johns Hopkins University

Investigators
Principal Investigator:     J Hang, MD, PhD     Johns Hopkins Medicine, Johns Hopkins University    
  More Information


Study ID Numbers:   04-03-05-05
First Received:   July 27, 2006
Last Updated:   July 27, 2006
ClinicalTrials.gov Identifier:   NCT00358241
Health Authority:   United States: Institutional Review Board

Keywords provided by Johns Hopkins University:
Nerve block, postoperative pain, analgesia  

Study placed in the following topic categories:
Signs and Symptoms
Postoperative Complications
Pain
Pain, Postoperative

Additional relevant MeSH terms:
Pathologic Processes

ClinicalTrials.gov processed this record on November 04, 2008




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