Completed

Evaluation of Experimental and Commercial Air-Activated, Adhesive Backed Heat Patches

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Thermal Adhesion Patch

+ Marketed Thermal Adhesion Patch

+ Placebo Patch

Device
Who is being recruted

From 18 to 70 Years
+30 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other Study

Placebo-Controlled
Interventional
Study Start: October 2012
See protocol details

Summary

Principal SponsorChattem, Inc.
Last updated: March 17, 2017
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2012

Actual date on which the first participant was enrolled.

A disposable, air-activated, adhesive backed heat patch is being developed to provide temporary relief from minor muscular ache and joint pains associated with overexertion strains and sprains as well as minor pain associated with arthritis. The aim of the study is to determine the safety and tolerability of the patch during normal wear conditions.

Principal SponsorChattem, Inc.
Last updated: March 17, 2017
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

40 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

Some studies explore topics that don't fall into a specific category. These might include innovative research, new technologies, or emerging healthcare areas.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 70 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

12 inclusion criteria required to participate
Participant's back region must be free of excessive hair, cuts, tattoos, or other aberrations

Participants are 18-70 years of age

Participants are willing to come in with a CLEAN back

Participants who are 55 years of age or older, agree to supply a t-shirt to wear at visit two that can be marked on with a marker

Show More Criteria

18 exclusion criteria prevent from participating
Participants unable to tolerate conditions of protocol

Participants viewed by the investigator as not being suitable for the study

Participants who are currently participating in another clinical trial

Participants who are pregnant or nursing, oral interview only

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

33.333% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
Group of subjects wearing the experimental patch for 8 hour study duration

Group II

Active Comparator
Group of subjects wearing comparative predicate device for 8 hour study duration.

Group III

Placebo
Group of subjects wearing the placebo patch for 8 hour study duration

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Radiant Research, Inc.

Pinellas Park, United StatesOpen Radiant Research, Inc. in Google Maps
CompletedOne Study Center