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Идёт набор NCT06427889

Treatment Effects of Two Pharmaceutical Skin Care Creams for Xerotic Feet Among Persons with Diabetes

Фаза IV С лечением Diabetes Mellitus Skin and Connective Tissue Diseases

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Canoderm, Oviderm, Decubal.
Кому может быть актуально
Состояния в реестре: Diabetes Mellitus, Skin and Connective Tissue Diseases. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Швеция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

A Superiority Study Comparing Two Pharmaceutical Skin Care Creams Containing Different Humectants with a Non-humectant Containing Skin Care Cream for the Treatment of Xerotic Foot of Persons with Diabetes

Обзор

Introduction Diabetic foot-ulcers leads to decreased quality of life, risk of major amputation, and resource demanding health-care. To minimize the risk of developing foot-ulcers, persons with diabetes are given the advice to daily inspect their feet and to apply skincare formulations. However, commercially available skincare products have rarely been developed and evaluated for diabetes foot care specifically. The primary aim of this randomized controlled trial (RCT) is to evaluate the effects in reducing foot xerosis in persons with diabetes without foot-ulcers using two skincare creams containing different humectants (interventions) against a cream base non-humectant (comparator). Secondary outcomes are to evaluate differences on skin barrier integrity, low-molecular weight biomarkers and skin microbiota, microcirculation including transcutaneous oxygen pressure, degree of neuropathy, and HbA1c between intervention-comparator cream. Methods Two-armed double-blind RCT. With 80% power, two-tailed significance of 2.5% in each arm, 39 study persons is needed in each arm, total 78 persons, to be able to prove a reduction of at least one category in the Xerosis Severity Scale with the intervention creams compared to the comparator. In one arm, each participant will treat one foot with one of the intervention creams (Oviderm® or Canoderm®), while the opposite foot will be treated with the comparator cream (Decubal® lipid cream®), twice a day. If needed, participants are enrolled after a wash-out period of two weeks. The participants will undergo examinations at baseline, day 14 and day 28. Discussion This RCT evaluate the potential effects of humectants in skin creams against foot xerosis in persons with diabetes. The outcomes of this trial could have implications on treatment recommendations of foot care and for the prevention of foot ulcer.

Вмешательства

  • Препарат Canoderm
    humectant
  • Препарат Oviderm
    humectant + antimicrobial
  • Препарат Decubal
    Non-humectant

Первичные конечные точки

  • Xerosis Severity [Срок оценки: 4 weeks]
Вторичные конечные точки (4)
  • Transepidermal water loss [Срок оценки: 4 weeks]
  • Skin resistance [Срок оценки: 4 weeks]
  • Skin Capacitance [Срок оценки: 4 weeks]
  • Skin pH [Срок оценки: 4 weeks]

Критерии участия

Критерии включения

  • Persons above 18 years of age diagnosed with diabetes mellitus, both type I and II, with self-experienced dry skin.
  • Dry skin on both feet with a Xerosis Severity Scale (XSS) score between two to six. No more than one XSS score in difference between the subjects' feet.
  • Ability to understand sufficient Swedish language to complete the necessary forms and understand the procedure of the study.

Критерии исключения

  • Known sensibility to any of the ingredients in the products.
  • Other diagnosed skin disease on the feet.
  • Active lesions on either foot.
  • Treatment with local medications, including topical moisturizers or keratolytic agents on the feet, within two weeks before the beginning of the study.
  • Potential study subjects judged unable to comply with treatment schedule and study specific information.
  • Female of childbearing potential that do not use effective medically accepted contraception.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Тройное слепое
Основная цель
Профилактика

Центры проведения

Швеция · 1 центр
  • Malmö University — Malmö

Публикации

  • Ericsson A, Borgstrom K, Kumlien C, Gershater Annersten M, Ruzgas T, Engblom J, Gudmundsson P, Lazer V, Jankovskaja S, Lavant E, Agren-Witteschus S, Bjorklund S, Salim S, Astrom M, Acosta S. Treatment effects of two pharmaceutical skin care creams for xerotic feet among persons with diabetes: Rationale and design of a two-armed double blind randomized controlled trial. Contemp Clin Trials Commun. PMID 39345688

Идентификаторы

NCT: NCT06427889 · 2022-500907-27-01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗