- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT04913636
Assessing Effects of a Denture Gel on Gum Abrasions
A Pilot Clinical Study to Determine the Effect Denture Gel Has on the Prevention of Gum Abrasions
Обзор исследования
Статус
Условия
Вмешательство/лечение
Подробное описание
This is a single center, two-treatment, parallel design study. Up to 40 subjects will be enrolled with a full mandibular and full maxillary denture with a history of food related abrasions.
At each visit, an Oral Soft Tissue exam, a Mucosa Condition Assessment and a Gum Abrasion Evaluation will be performed. At Baseline, the subjects will be randomized to a treatment group. At Baseline, Week 2, and Week 4 subjects will be asked to eat 20 grams of peanuts 4 times for a total consumption of 80 g of peanuts (subjects will be permitted to take breaks if needed and drink small sips of water). Following the peanut challenge, a licensed dental professional will re-evaluate the number and size of abrasions. Subjects will receive a consumer questionnaire to complete as well prior to the Baseline, Week 2, and Week 4 assessments.
Тип исследования
Регистрация (Действительный)
Фаза
- Непригодный
Контакты и местонахождение
Места учебы
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Indiana
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Fort Wayne, Indiana, Соединенные Штаты, 46825
- Salus Research
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-
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
In order to be included in the study, each subject must:
- Be 18 years of age;
- Read, sign, and receive a copy of the Informed Consent prior to initiation of study procedures;
- Have a full maxillary and mandibular denture and wear on a daily basis;
- Have a history of food particles getting under their full denture and causing gum irritation;
- Are willing to abstain from eating at least four hours prior to the visits;
- Are willing to eat 4 X 20 grams of peanuts three times (Baseline, Week 2 and Week 4) without denture adhesive;
- Clean their dentures on a daily basis;
- Agree not to change their regular denture cleaning routine;
- Agree to abstain from using denture adhesive during the study;
- Agree to not participate in any other oral/dental product studies during the study.
Exclusion Criteria:
- Exhibit evidence of obvious oral pathology, as determined by the Study Dentist, as a result of a mandatory OST examination on the first day of the study;
- Are allergic to any of the ingredients contained in the study product gel;
- Are allergic to peanuts;
- Wear dentures overnight;
- Are insulin-dependent and/or have any health condition(s) which would prevent compliance with study procedures;
- Are routinely using denture adhesive;
- Present with any disease or conditions that could be expected to increase their susceptibility to gum abrasion (like diabetes or xerostomia); or
- Present with any disease or conditions that could be expected to interfere with examination procedures or the subject's safe completion of the study
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Профилактика
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Одинокий
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Фальшивый компаратор: Контрольная группа
|
Subjects will perform their regular denture cleaning routine.
|
|
Экспериментальный: Тестовая группа
|
In the evening subjects will perform their regular denture cleaning routine.
They will be instructed to sleep without dentures.
Subjects will rinse out their mouth with water (if subjects brush their oral mucosa with brush, they will be allowed to continue doing so) and apply the gel to their mucosa where they normally wear upper or lower denture.
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Abrasion Assessment (Number)
Временное ограничение: Day 3
|
The total number of abrasions pre-food challenge
|
Day 3
|
|
Abrasion Assessment (Size)
Временное ограничение: Day 3
|
The average size/area (in mm) of the total number of abrasions pre-food challenge
|
Day 3
|
|
Abrasion Assessment (Number)
Временное ограничение: Day 6
|
The total number of abrasions pre-food challenge
|
Day 6
|
|
Abrasion Assessment (Number)
Временное ограничение: Week 2
|
The total number of abrasions pre-food challenge
|
Week 2
|
|
Abrasion Assessment (Number)
Временное ограничение: Week 4
|
The total number of abrasions pre-food challenge
|
Week 4
|
|
Abrasion Assessment (Size)
Временное ограничение: Day 6
|
The average size/area (in mm) of the total number of abrasions pre-food challenge
|
Day 6
|
|
Abrasion Assessment (Size)
Временное ограничение: Week 2
|
The average size/area (in mm) of the total number of abrasions pre-food challenge
|
Week 2
|
|
Abrasion Assessment (Size)
Временное ограничение: Week 4
|
The average size/area (in mm) of the total number of abrasions pre-food challenge
|
Week 4
|
|
Mucosal Assessment
Временное ограничение: Day 3
|
The mucosal region under the denture was assessed with one score per arch (two total arches) each arch is scored ranging from 0(better) - 3(worse). The scores are then summed for a total score. The scale is measured as follows: 0 = pink firm tissue absent of redness and inflammation; 1 = mild redness or inflammation - slight change in color and little change in texture; 2 = moderate redness and/or inflammation - moderate glazing, redness, edema and hypertrophy 3 = severe redness and/or inflammation - marked redness and hypertrophy. |
Day 3
|
|
Mucosal Assessment
Временное ограничение: Day 6
|
The mucosal region under the denture was assessed with one score per arch (two total arches) each arch is scored ranging from 0(better) - 3(worse). The scores are then summed for a total score. The scale is measured as follows: 0 = pink firm tissue absent of redness and inflammation; 1 = mild redness or inflammation - slight change in color and little change in texture; 2 = moderate redness and/or inflammation - moderate glazing, redness, edema and hypertrophy 3 = severe redness and/or inflammation - marked redness and hypertrophy. |
Day 6
|
|
Mucosal Assessment
Временное ограничение: Week 2
|
The mucosal region under the denture was assessed with one score per arch (two total arches) each arch is scored ranging from 0(better) - 3(worse). The scores are then summed for a total score. The scale is measured as follows: 0 = pink firm tissue absent of redness and inflammation; 1 = mild redness or inflammation - slight change in color and little change in texture; 2 = moderate redness and/or inflammation - moderate glazing, redness, edema and hypertrophy 3 = severe redness and/or inflammation - marked redness and hypertrophy. |
Week 2
|
|
Mucosal Assessment
Временное ограничение: Week 4
|
The mucosal region under the denture was assessed with one score per arch (two total arches) each arch is scored ranging from 0(better) - 3(worse). The scores are then summed for a total score. The scale is measured as follows: 0 = pink firm tissue absent of redness and inflammation; 1 = mild redness or inflammation - slight change in color and little change in texture; 2 = moderate redness and/or inflammation - moderate glazing, redness, edema and hypertrophy 3 = severe redness and/or inflammation - marked redness and hypertrophy. |
Week 4
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Соавторы и исследователи
Спонсор
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Другие идентификационные номера исследования
- 2020089
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .
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