Management of the Sprained Ankle by Help of NSAID-Plaster - Tabular View

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

Tracking Information

First Received Date ^†

January 31, 2006

Last Updated Date

March 10, 2006

Start Date ^†

February 2006

Current Primary Outcome Measures ^†

Pain-score

Original Primary Outcome Measures ^†

Same as current

Change History

Complete list of historical versions of study NCT00284765 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^†

Original Secondary Outcome Measures ^†

Descriptive Information

Brief Title ^†

Management of the Sprained Ankle by Help of NSAID-Plaster

Official Title ^†

Optimation of Treatment of the Sprained Ankle by Help of NSAID-Plaster (Flector). A Questionnaire.

Brief Summary

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.

Detailed Description

Study Phase

Study Type ^†

Interventional

Study Design ^†

Randomized, Open Label, Active Control, Parallel Assignment

Condition ^†

The Sprained Ankle

Intervention ^†

Procedure: flector

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 ^†

Recruiting

Enrollment ^†

200

Completion Date

May 2006

Primary Completion Date

Eligibility 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

Gender

Both

Ages

18 Years and older

Accepts Healthy Volunteers

Contacts ^††

Contact: Berit Jørgensen

bekajo@fks.vejleamt.dk

Location Countries ^†

Denmark

Expanded Access Status

Administrative Information

NCT ID ^†

NCT00284765

Responsible Party

Secondary IDs ^††

Study Sponsor ^†

Kolding Sygehus

Collaborators ^††

Investigators ^†

Principal Investigator:

Berit Jørgensen, MD

Kolding Sygehus

Information Provided By

Kolding Sygehus

Verification Date

January 2006

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