NCT01841788已完成不适用
Evaluation of Experimental and Commercial Air-Activated, Adhesive Backed Heat Patches
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 2
- 主要终点
- Irritation Evaluation
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Participants are 18-70 years of age;
- •must be in general good health;
- •must have absence of any visible disease that might be confused with a skin reaction to the test material;
- •Participant's back region must be free of excessive hair, cuts, tattoos, or other aberrations;
- •must understand and sign Informed Consent;
- •must be considered dependable and able to follow directions;
- •must be willing to restrict their activity for the 8 hour patch wear time so that the patches/thermocouples do not come loose;
- •must be willing to wear a pouch containing the thermostat and thermocouple wiring for the entire 8 hour period and to return all study supplies to the site at Visit
- •If the items are not returned subject may be invoiced for the value of the unit;
- •must be willing not to use any topical products such as lotions, sunscreens, etc. in the test area while participating on the study;
- •must agree to use an adequate means of birth control which include: abstinence, partner vasectomy, Intrauterine Device, hormonal implant devices/injections, regular use of birth control pills, birth control patches or condoms with a spermicidal agent;
- •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.
排除标准
- •Participants with known skin sensitivity to adhesion products;
- •Participants with any skin abnormality likely to be aggravated by the study material such as dermatological disease or infection, rash, atrophic, fragile, or abnormally dry skin, cuts or abrasions at the treatment site;
- •Participants who are pregnant or nursing, oral interview only;
- •Participants with diabetes or poor circulation;
- •Participants unable to tolerate conditions of protocol;
- •Participants viewed by the investigator as not being suitable for the study;
- •Participants who have had active skin cancer including basal cell carcinoma, or other cancer within one year;
- •Participants who are currently participating in another clinical trial;
- •Participants who routinely use anti-inflammatory medications (within 5 days of study start (81mg Aspirin is okay)) or immunosuppressive or antihistamine medications within 3 weeks prior to study start (steroid nose/eye drops are ok);
- •Participants who currently use allergy injections;
- •Participants with history of severe asthma;
- •Participants with active or uncontrolled immunologic disorders i.e. AIDS, HIV positive, systemic lupus erythematosus, rheumatoid arthritis;
- •Participants with uncontrolled thyroid disease;
- •Participants who have any clinically significant chronic illness which could place the subject at increased risk during participation or result in inappropriate dermal response during the study;
- •Participants who have used topical medications at the test sites within the past 14 days;
- •Participants who have lower midline abdominal pinnicula which may interfere with heat patch/wrap application or evaluation;
- •Participants who have a pacemaker, defibrillator or other implantable medical device;
- •Participants who have allergies to latex, polyethylene, polypropylene, nickel, chromium or aluminum.
结局指标
主要结局
Irritation Evaluation
时间窗: 8 hours
A trained skin grader will apply a predetermined scale to the observed skin reactions in the test areas under light supplied by a 100-watt incandescent blue bulb.
次要结局
- Adhesion Evaluation(8 Hours)
研究者
研究点 (2)
Loading locations...
相似试验
终止
不适用
A Comparative Study to Evaluate Two Air-Activated Adhesive Backed Heat PatchesHealthyNCT02080143Chattem, Inc.200
终止
不适用
Mask Adhesive Institutional StudyCovid19Respiratory FailureNCT04644276Philips Clinical & Medical Affairs Global7
已完成
不适用
Evaluation of Experimental and Commercial Air-Activated, Adhesive Backed Heat PatchesEffects of HeatTolerabilityAdhesivenessDermal IrritationNCT01841801Chattem, Inc.157
已完成
不适用
Clinical Performance of the Embrace Isothermal MattressHypothermiaNCT01425086Stanford University36
已完成
不适用
Safety and Performance of Newly Developed 1-piece Ostomy Product Compared With SenSuraIleostomy - StomaNCT01799239Coloplast A/S32