Hydrogel Blister Patch Prototype Treatment for Foot Blisters on the Heel

Blister Clinical Trial

Official title:

Feasibility Study to Evaluate the Safety and Performance of a Hydrogel Blister Patch Prototype for the Treatment of Foot Blisters

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01088685
• Other study ID #: UNKEDI0001
• Status: Completed
• Phase: N/A
• First received: March 16, 2010
• Last updated: October 4, 2011
• Start date: March 2010
• Est. completion date: November 2010

Study information

• Verified date: October 2011
• Source: Johnson & Johnson Consumer and Personal Products Worldwide
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: German Institute of Medical Documentation and Information
• Study type: Interventional

Clinical Trial Summary

Study to evaluate the safety and performance of a new blister patch intended to treat blisters on the heel of the foot.

Description:

The study will require participation for up to 14 days of participation or less if the blister heals sooner, will recruit 100 subjects with fluid filled blisters on the heel of the foot that are intact and not broken. Some subjects will be asked to have their blisters photographed. All subjects will be required to have their blister unroofed (top layer of skin removed by the physician using sterile instruments). All subjects will receive study product, either test product or a marketed product.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 93
• Est. completion date: November 2010
• Est. primary completion date: November 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female subjects, 18 years of age or older;

• Individuals who are willing and able to provide informed consent

• Female subjects of child bearing potential must have a negative urine pregnancy test prior to application of the study products;

• Females of childbearing potential must be using a medically-acceptable method of birth control for at least one month prior to Visit 1 such as the ones listed below and agree to continue using this method during their participation in the study; Note that abstinence is not an approved method of birth control.

• Postmenopausal or amenorrheic for one year

• Surgically sterile (hysterectomy, tubal ligation, or oophorectomy)

• Use of an effective method of birth control (e.g. prescription oral contraceptives, contraceptive implants or injections, intrauterine device, diaphragm, cervical cap or condoms with spermicide)

• Individuals exhibit a blister on the heel that is determined by the investigator to be no more than 72 hours old and in stage 2

• Subject is willing to have blister unroofed (top layer of blister removed) by the investigator

• Subject is willing and able to follow the study directions, to participate in the study, and to return for all specified visits

Exclusion Criteria:

• Pregnant, planning a pregnancy or actively nursing

• Exhibits a foot blister on the heel that exceeds 1125mm2 or would otherwise not be covered by the hydrogel portion of the study product

• Unstable or uncontrolled medical conditions that could require intensive treatment during the course of the study

• Individuals with autoimmune disorders including, but not limited to, lupus erythematosus, rheumatoid arthritis, or HIV/AIDS

• Currently participating in or, within the past 30 days have participated in another clinical study using an investigational drug or device

• Employees of the site, or friends/relatives of employees that would have access to study information

• Diabetic, type I or type II

• Treatment for any type of cancer within the last 2 years or history of skin cancer

• Damaged skin in or around test sites, which include sunburn, extremely deep tans, uneven skin tones, tattoos, scars, excessive hair, numerous freckles, acne, and disfiguration of the test site

• History of clinically determined allergic reaction or irritation to any of the test product ingredients

• History of or known allergy to iodine

• Currently taking or expected to take any of the following during the course of the study: amphetamines, benzodiazepines, cocaine, marijuana, methaqualone, methadone, opiates, propoxyphene, barbiturates, and phencyclidine

• Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Blister

Intervention

Device:
• Experimental Blister Patch
Experimental hydrogel blister patch to be applied as needed (at least every 2 days) consecutively until blister heals
• Marketed Pflaster
Foot Blister Patch to be applied as needed (at least every 2 days) until blister heals

Locations

Country	Name	City	State
Germany	SCIderm GmbH	Hamburg

Sponsors (1)

Lead Sponsor	Collaborator
Johnson & Johnson Consumer and Personal Products Worldwide

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Investigator Assessment	Global assessment of the product by the investigator at the subject's last visit.	at subject's last visit, within 14 days of start	No
Secondary	Subject Assessment	Global assessment of the product by the subject at the subject's last visit.	at subject's last visit, within 14 days of start	No
Secondary	Time to Heal	Record of the time it took for the blister to heal within the 14-day study period.	Baseline to subject's last visit, within 14 days of start	No