The Prevalence of Contact Allergies for Wound Dressings In Patients With Diabetic Foot Ulcers (PAID Study) (PAID)

The Prevalence of Contact Allergies for Wound Dressings In Patients With Diabetic Foot Ulcers

Rationale: Foot ulcers among diabetics are common. The presence of a contact allergy limits the healing process. Contact allergies for wound dressings are common among patients with ulcers caused by venous insufficiency but less is known about contact allergies in diabetic patients with ulcers.

Objective: To determine the prevalence of contact allergies for wound dressings in patients with diabetic foot ulcers.

Study design: A prospective multicenter study.

Study population: Patients (n=139) with diabetic foot ulcers caused by type 1 or 2 diabetes mellitus treated at Rijnstate Hospital Arnhem, the Netherlands.

Main study parameters/endpoints: The primary study parameter is the presence of contact allergies for wound dressings.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: An allergy test is standard procedure at Rijnstate Hospital, there is no direct technique-related burden or risk for the patient. In addition, wound dressings can be adjusted in patients where a contact allergy is determined which will benefit the prognosis of these patients. The data of this study will give insight in the prevalence of contact allergies for wound dressings in patients with diabetic foot ulcers.

Study Overview

• Status: Recruiting
• Conditions: Diabetic Foot; Contact Allergy
• Intervention / Treatment: Diagnostic test: PATCH test

Detailed Description

Foot ulcers among diabetics are common. In 2015, around 20,000 patients in the Netherlands had a diabetic foot ulcer.1 A study using data from Dutch general practices found a prevalence rate of 0.50% and a 4-year prevalence rate of 2.85%.2 For Europe, Zhang et al. estimated a pooled prevalence of 5.1% (95%CI: 4.1-6.0%).3 Prevalence rates increase with age.

The underlying mechanism of diabetic foot ulcers is most often solely neuropathy (60 to 70%), 15 to 20% have peripheral artery disease (PAD) only, and 15 to 20% have a mixture of both.4 Diabetic foot is more prevalent in males and more prevalent in type 2 diabetes than in type 1 diabetes3. Ulcers in patients without diabetes are mostly caused by venous insufficiency.5

Ulcers have a slow healing tendency. Around 15 percent of diabetic patients with an ulcer eventually have to amputate (a part of) the leg.1 Good wound care is therefore important. However, wound care can be delayed in the presence of a contact allergy. Contact allergy (synonym for contact sensitivity) is defined as an altered immune status of an individual induced by a particular sensitizing substance, a contact allergen. An individual in whom contact allergy has been induced will develop a secondary immune response if there is skin exposure to the same (or cross-reacting) allergen. This process is called elicitation, and will manifest as allergic contact dermatitis (type IV hypersensitivity).6 Allergic contact dermatitis, also termed allergic contact eczema, is defined as an inflammatory skin reaction caused by direct contact with noxious agents in the environment as a result of contact allergy.

Among patients with venous leg ulcers contact allergies is seen in around 50 percent of which 10-20% for wound dressings.7-10 The prevalence of contact allergies is getting higher and also increasing with the duration of the ulcer. 8,10 Wound dressings can cause allergic contact eczema (allergic contact dermatitis).

At present, the prevalence of contact allergies for wound dressings in diabetic patients with foot ulcers is unknown. With this study we want to gain insight in the prevalence of contact allergies in patients with diabetic foot ulcers and investigate if the prevalence of contact allergies among diabetic patients is as high as the prevalence in patients with venous leg ulcers.

Objective of the study:

The primary objective of this study is to determine the prevalence of contact allergies in patients with diabetic foot ulcers.

Study design:

This is a prospective, multi-centre study.

Study population:

The study population are high risk diabetic patients with a foot ulcer visiting the multidisciplinary consultation hour for diabetics at the clinic.

Diabetic patients are patients diagnosed with type 1 or type 2 diabetes.

Primary study parameters/outcome of the study:

The presence of contact allergy for wound dressings

Secundary study parameters/outcome of the study (if applicable):

The following factors will be gathered at baseline:

• Age
• Gender
• Diabetes type
• Duration of diabetes
• Medication use
• Ulcer characteristics like type, size, duration, progress (TEXAS classification)
• Number of past foot ulcers
• Duration of past foot ulcers
• Known allergies or atopy constitution
• Presence of allergic contact dermatitis around the wound
• Doses corticosteroid or antihistaminic therapy (not during PATCH testing)
• History of eczema

Parameters to define if there are other mechanisms besides diabetics underlying the ulcer:

• Ankle brachial index , toe pressure measurement or Transcutaneous oxygen pressure (TcPo2)
• Venous insufficiency which is measured by a venous duplex, if applicable

Parameters related with contact allergy or parameters that can influence the development of a contact allergy:

• Known allergy. If yes, which allergy/allergies?
• Duration of current ulcus cruris
• Number of past ulcers

• Treatment with wound dressing(s) current episode:

  • Duration of ulcer
• Treatment with wound dressing(s) prior episode(s)
• Prevalence of allergic contact dermatitis

Nature and extent of the burden and risks associated with participation, benefit and group relatedness (if applicable):

Not applicable

• Study Type: Observational
• Enrollment (Anticipated): 139

Contacts and Locations

• Study Contact: Name: Birgitte Visch, MD; Phone Number: 0031 (0)88-0055081; Email: bvisch@rijnstate.nl

Study Locations

• Netherlands
  • Gelderland
    • Arnhem, Gelderland, Netherlands, 6800 TA
      • Recruiting
      • Rijnstate
      • Contact: Birgitte Visch, MD; Phone Number: 0031 (0)88-0055081,; Email: bvisch@rijnstate.nl

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Probability Sample

Study Population

The study population are high risk diabetic patients with a foot ulcer visiting the multidisciplinary consultation hour for diabetics at the clinic.

Diabetic patients are patients diagnosed with type 1 or type 2 diabetes.

Description

Inclusion Criteria:

• Age of 18 years or older;
• Diagnosed with type 1 or 2 diabetes mellitus;
• Diagnosed with diabetic foot ulcer;
• Provided written informed consent.

Exclusion Criteria:

• Patient unwilling or unlikely to comply with the study procedures
• Patient receiving systemic corticosteroid therapy during PATCH testing (patient should stop with corticosteroid therapy three days before PATCH testing, and may start when testing and reading is done)
• Patient receiving antihistaminic therapy during PATCH testing (patient should stop with antihistaminic therapy three days before PATCH testing, and may start when testing and reading is done)

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Patients with diabetic foot ulcers; All patients with diabetic foot ulcers will undergo a PATCH test to determine the prevalence of contact allergies against wound dressings.	Diagnostic test: PATCH test; The PATCH test is a method used to determine whether a specific substance causes allergic inflammation of a patient's skin, in this case contact allergy for wound dressings. Two days after PATCH test is applied, the patches are removed. The next day, the presence of a contact allergy is determined.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Presence of contact allergy for wound dressings	The presence of contact allergy for wound dressings	3 days after application of PATCH test

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Presence of eczema	Presence of eczema/dermatitis	Collected at baseline

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Ulcer duration	Duration of ulcers	Collected at baseline
Past ulcers	The number of ulcers in the past	Collected at baseline

Collaborators and Investigators

• Sponsor: Rijnstate Hospital
• Investigators: Principal Investigator: Birgitte Visch, MD, Rijnstate

Study record dates

Study Major Dates

• Study Start (Actual): September 17, 2019
• Primary Completion (Anticipated): December 1, 2022
• Study Completion (Anticipated): December 1, 2022

Study Registration Dates

• First Submitted: September 9, 2019
• First Submitted That Met QC Criteria: September 9, 2019
• First Posted (Actual): September 11, 2019

Study Record Updates

• Last Update Posted (Actual): October 18, 2021
• Last Update Submitted That Met QC Criteria: October 15, 2021
• Last Verified: October 1, 2021

More Information

Terms related to this study

• Keywords: Wound Dressing
• Additional Relevant MeSH Terms: Cardiovascular Diseases; Vascular Diseases; Skin Diseases; Immune System Diseases; Endocrine System Diseases; Diabetic Angiopathies; Leg Ulcer; Skin Ulcer; Diabetes Complications; Diabetes Mellitus; Diabetic Neuropathies; Foot Diseases; Dermatitis; Skin Diseases, Eczematous; Hypersensitivity, Delayed; Dermatitis, Contact; Hypersensitivity; Diabetic Foot; Foot Ulcer; Dermatitis, Allergic Contact
• Other Study ID Numbers: PAID study

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No