This site became the new on June 19th. Learn more.
Show more Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu
Give us feedback

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
Information provided by:
Kolding Sygehus Identifier:
First received: January 31, 2006
Last updated: March 10, 2006
Last verified: January 2006
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

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

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
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 identifier: NCT00284765

Contact: Berit Jørgensen

Kolding Sygehus Recruiting
Kolding, Denmark
Contact: Berit Jørgensen, MD   
Principal Investigator: Berit Jørgensen, MD         
Sponsors and Collaborators
Kolding Sygehus
Principal Investigator: Berit Jørgensen, MD Kolding Sygehus
  More Information Identifier: NCT00284765     History of Changes
Other Study ID Numbers: VF-20050182
Study First Received: January 31, 2006
Last Updated: March 10, 2006

Additional relevant MeSH terms:
Ankle Injuries
Leg Injuries
Wounds and Injuries
Diclofenac hydroxyethylpyrrolidine
Anti-Inflammatory Agents, Non-Steroidal
Analgesics, Non-Narcotic
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 processed this record on September 21, 2017