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Management of the Sprained Ankle by Help of NSAID-Plaster

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified January 2006 by Kolding Sygehus.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00284765
First Posted: February 1, 2006
Last Update Posted: March 13, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Kolding Sygehus
  Purpose
The purpose of this trial is to study the management of the sprained ankle by help of NSAID-plaster. A questionnaire. The effect of RICE and RICE + NSAID-plaster in the treatment of the sprained ankle, compared by pain-score.

Condition Intervention
The Sprained Ankle Procedure: flector

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Official Title: Optimation of Treatment of the Sprained Ankle by Help of NSAID-Plaster (Flector). A Questionnaire.

Resource links provided by NLM:


Further study details as provided by Kolding Sygehus:

Primary Outcome Measures:
  • Pain-score

Estimated Enrollment: 200
Study Start Date: February 2006
Estimated Study Completion Date: May 2006
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • A sprained ankle, less than 24 hours old, understanding Danish, 18 years or older

Exclusion Criteria:

  • Fracture of the ankle, wound around the ankle, allergy of NSAID- pregnancy, daily use of NSAID, GI-bleeding
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00284765


Contacts
Contact: Berit Jørgensen bekajo@fks.vejleamt.dk

Locations
Denmark
Kolding Sygehus Recruiting
Kolding, Denmark
Contact: Berit Jørgensen, MD       bekajo@fks.vejleamt.dk   
Principal Investigator: Berit Jørgensen, MD         
Sponsors and Collaborators
Kolding Sygehus
Investigators
Principal Investigator: Berit Jørgensen, MD Kolding Sygehus
  More Information

ClinicalTrials.gov Identifier: NCT00284765     History of Changes
Other Study ID Numbers: VF-20050182
First Submitted: January 31, 2006
First Posted: February 1, 2006
Last Update Posted: March 13, 2006
Last Verified: January 2006

Additional relevant MeSH terms:
Ankle Injuries
Leg Injuries
Wounds and Injuries
Diclofenac hydroxyethylpyrrolidine
Diclofenac
Anti-Inflammatory Agents, Non-Steroidal
Analgesics, Non-Narcotic
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Inflammatory Agents
Antirheumatic Agents
Cyclooxygenase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action