Effectiveness of Infiltrations in the Treatment of Plantar Fasciopathy
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: Infiltration, Conservative treatment.
- Кому может быть актуально
- Состояния в реестре: Plantar Fasciitis of Both Feet, Plantar Fasciopathy. Базовые параметры: 18 лет — 50 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
- Испания
- 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
Effectiveness of Infiltrations in the Treatment of Plantar Fasciopathy: A Randomized Clinical Study.
Обзор
This clinical study aims to evaluate the effectiveness of infiltrations in the treatment of plantar fasciopathy, a painful condition that affects the sole of the foot and is common in active people. Plantar fasciopathy is caused by inflammation or damage to the plantar fascia, the tissue that connects the heel to the toes. Participants in this study will be randomly assigned to receive one of two treatments: corticosteroid infiltrations or conservative treatment without infiltrations. Infiltrations will be guided by ultrasound to ensure accuracy. The study will evaluate pain reduction and improvement in foot function over a six-month period. The objective of the study is to determine if infiltrations provide a significant improvement compared to other non-invasive treatments. The results will help doctors and patients make informed decisions about the best treatment options for plantar fasciopathy.
Подробное описание
This clinical study, titled \"Effectiveness of Infiltrations in the Treatment of Plantar Fasciopathy\", will be carried out at the University of Seville and its main objective is to evaluate the impact of corticosteroid infiltrations on pain reduction and functional improvement in patients diagnosed with plantar fasciopathy.
Вмешательства
- Препарат Infiltration
The intervention consists of the administration of infiltrations in the affected plantar fascia of participants with a diagnosis of plantar fasciopathy. A drug such as a corticosteroid, PRP or hyaluronic acid will be used, which will be injected under ultrasound guidance to ensure precision at the site of the injury. This intervention aims to reduce inflammation and pain, thus improving the functionality of the foot. Up to three infiltrations will be performed, depending on the patient\& - Другое Conservative treatment
The control group is used to compare the effectiveness of infiltrations with a non-invasive approach in the treatment of plantar fasciopathy. This group will not receive any infiltration and will focus on conservative interventions.
Первичные конечные точки
- Change in Pain Level [Срок оценки: Evaluations will be carried out at the beginning of the study, and at 3, 6 and 12 weeks after the intervention.]
Вторичные конечные точки (1)
- Functional Improvement [Срок оценки: Evaluations at the beginning, and at 3, 6 and 12 weeks post-intervention.]
Критерии участия
Критерии включения
Age: Participants aged 18 to 50 years. Diagnosis: Confirmed diagnosis of plantar fasciopathy based on clinical evaluation and imaging (if applicable).
Duration of Symptoms: Symptoms persisting for at least 6 weeks prior to enrollment.
Pain Level: Reported pain level of at least 4 on the Visual Analog Scale (VAS) at baseline.
Ability to Comply: Participants must be able to follow study protocols and attend follow-up appointments.
Informed Consent: Participants must provide written informed consent to participate in the study.
Критерии исключения
Other Foot Pathologies: Presence of other significant foot conditions (e.g., fractures, arthritis, tarsal tunnel syndrome) that could interfere with the study results.
Pregnancy or Breastfeeding: Pregnant or breastfeeding individuals will be excluded from the study.
Neurological Disorders: History of significant neurological disorders affecting lower limb function.
Systemic Conditions: Patients with systemic conditions (e.g., diabetes, autoimmune diseases) that could affect healing or response to treatment.
Allergy to Corticosteroids: Known allergy or adverse reaction to corticosteroids or local anesthetics.
Psychiatric Disorders: Individuals with severe psychiatric disorders that may impair their ability to provide informed consent or adhere to the study protocol.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Перекрёстный дизайн
- Маскирование
- Простое слепое
- Основная цель
- Лечение
Центры проведения
Испания · 1 центр
- Universidad de Sevilla — Seville
Идентификаторы
NCT: NCT06671223 · TFMAGM · TFMAGM2024