- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01843088
Trial of Mannitol Cream for Pain Relief After a Long Run (PainCream)
October 10, 2013 updated by: University of British Columbia
Randomized Trial of Mannitol Cream for Pain Relief After a Long Run
Mannitol cream has been shown clinically to be effective for pain control.
To determine if this effect is worth testing on a larger scale, 170 runners will receive a sample of 25% mannitol cream to apply on one leg, and the cream base without the mannitol on the other leg following a 10 km or longer run, and for the following five days.
Mannitol and control legs will be chosen at random for each runner.
Pain scores before and after cream application will be acquired each day for each leg.
Means and standard deviations found will be used to determine the size of a larger study.
Study Overview
Detailed Description
The hypothesis for this study is that Mannitol cream will reduce post long run pain more than vehicle cream alone.
In this parallel design, 170 runners who usually experience a pain level greater than 5/10 on a numerical rating scale from 0 to 10 where zero is no pain and 10 is the worst pain ever, will be given a cream containing 25% mannitol to apply on one leg and the vehicle cream to apply on the other leg.
The cream assignment will be randomized, and the runner, the person supplying the cream and the person inputting the data will be blinded as to which leg received which cream.
Pain levels in each leg following the long run will be recorded, via an e-mail questionnaire, or, failing this, by telephone, the day of the run, and each day, for five days following the run.
Mean and standard deviations for pain levels will be calculated for each treatment leg, and a repeated measures ANOVA (Analysis Of VAriance) will be done comparing the pain levels in each leg over the six days.
Using this information, if the NRS (Numeric rating scale) pain levels differ by more than 1/10 between the two groups, a larger study will be conducted using the information gathered in this study to determine sample size.
Study Type
Interventional
Enrollment (Actual)
170
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
British Columbia
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Vancouver, British Columbia, Canada, V7M 2K2
- Dr. Helene Bertrand, University of British Columbia, Department of Family Practice
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 74 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
either:
- never ran 10 km or more, or;
- NRS pain level greater than 5/10 in both legs following a 10 km or more run
Exclusion Criteria:
- no major skin allergies
- no allergy to mannitol
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mannitol cream
cream containing 25% mannitol, applied as often and as much as needed to one leg ( chosen at random), on the day of a 10 km run, following the run and for five days afterwards
|
25% mannitol in PENcream (See above) (See above) This will be applied as needed to one side of the body (blinded assignment) over painful painful areas of legs following a 10 km run, on the day of the run and for five days afterwards.
Other Names:
|
|
Placebo Comparator: Placebo cream
Same carrier cream as that containing the active ingredient, mannitol, but without the active ingredient.
Placebo cream to be applied to the painful areas of the other leg, chosen at random, on the day of a 10 km or more race, following the race, and as needed for the five days after the race.
It is to be noted that, as almost no mannitol is absorbed through the skin, it is highly unlikely that this would involve the pain levels in the placebo leg.
|
This is the vehicle only cream (PENcream) (See above) This will be applied as needed to one side of the body (blinded assignment) over painful painful areas of legs following a 10 km run, on the day of the run and for five days afterwards.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in NRS (Numeric rating scale) pain score
Time Frame: For six days following run
|
NRS (Numeric rating scale) pain score from zero, no pain, to 10 worst pain ever.
Change in pain score will be measured daily starting on day of race, comparing pain following the race, prior to the first cream application, to the daily scores for the subsequent five days.
Pain levels in leg given mannitol cream, and leg given placebo cream will be compared according to the change in their pain scores.
|
For six days following run
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
side effects of cream
Time Frame: For six days, starting on day of race.
|
Description of side effects by subjects.
The only likely to side effect would be a contact dermatitis as percutaneous systemic absorption of mannitol is negligible.
We will therefore monitor for contact dermatitis, and record its incidence, should it happen in this small sample.
In our experience with over 400 recipients, there have been no cases of contact dermatitis.
|
For six days, starting on day of race.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Helene Bertrand, MD, CCFP, University of British Columbia
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2013
Primary Completion (Actual)
May 1, 2013
Study Completion (Actual)
July 1, 2013
Study Registration Dates
First Submitted
April 16, 2013
First Submitted That Met QC Criteria
April 25, 2013
First Posted (Estimate)
April 30, 2013
Study Record Updates
Last Update Posted (Estimate)
October 11, 2013
Last Update Submitted That Met QC Criteria
October 10, 2013
Last Verified
October 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H13-00106
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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