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Набор скоро начнётся NCT07398651

Apremilast and Adalimumab in Psoriatic Arthritis Patients

Без фазы С лечением Psoriatic Arthritis Ultrasound Assessment TNF

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: Adalimumab, Apremilast.
Кому может быть актуально
Состояния в реестре: Psoriatic Arthritis, Ultrasound Assessment, TNF. Базовые параметры: 18 лет — 70 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
Египет
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Comparative Study Between Apremilast and Adalimumab in Psoriatic Arthritis Patients

Обзор

The aim of this work is to compare the efficacy of Apremilast combined with Methotrexate versus Adalimumab combined with Methotrexate

Подробное описание

Psoriatic arthritis is a heterogeneous chronic systemic auto-immune disease, with variable musculoskeletal involvement as well as skin and nail disease . Up to 30% of patients with psoriasis may develop Psoriatic arthritis over the course of their lifetime. Musculoskeletal manifestations of Psoriatic arthritis include peripheral arthritis, spondylitis, dactylitis and enthesitis.

The pathogenesis of Psoriatic arthritis is still unclear, due to the heterogeneity of the pathogenic pathways involved, the variable clinical manifestations, and different responses to treatment.

A predisposing genetic background in the presence of environmental factors, such as infections, microbiota (dysbiosis), obesity, biomechanical stress could activate the immune system and precipitate the onset of the disease.

Objectives:

* Assessment of the effect of the studied drugs on the disease activity clinically and laboratory in PsA patients. * Assessment of the effect of the studied drugs on functional status of PsA patients. * Evaluation of the effect of the studied drugs on the musculoskeletal ultrasound findings of PsA patients

Objectives:

* Assessment of the effect of the studied drugs on the disease activity clinically and laboratory in PsA patients. * Assessment of the effect of the studied drugs on functional status of PsA patients. * Evaluation of the effect of the studied drugs on the musculoskeletal ultrasound findings of PsA patients

Musculoskeletal ultrasound is considered one of the most important tools in studying the effects of rheumatic diseases on musculoskeletal structures.

It is demonstrated that ultrasound is more sensitive than conventional radiography and clinical examination for the assessment of inflammatory and structural changes in inflammatory arthritis, including Psoriatic arthritis, and particularly synovitis, enthesitis, tenosynovitis, and bursitis.

The treatment of Psoriatic arthritis requires attention to the active domains present in each patient. If the major active domain is peripheral arthritis, treatment usually begins with non-steroidal anti-inflammatory drugs to control symptoms of pain and mild inflammation. If these drugs fail to control disease activity, a conventional synthetic DMARDs is usually prescribed, most commonly methotrexate. Leflunomide and sulfasalazine have also been used in the management of peripheral joint disease. The European Alliance of Associations for Rheumatology guidelines on the management of Psoriatic arthritis with drug therapies suggest that if patients do not attain a satisfactory response

Вмешательства

  • Препарат Adalimumab
    PsA patients who will receive Adalimumab with methotrexate therapy for 3 months
  • Препарат Apremilast
    PsA patients who will receive Apremilast with methotrexate therapy for 3 months

Первичные конечные точки

  • Disease Activity Index for Psoriatic Arthritis [Срок оценки: 3 months]
Вторичные конечные точки (2)
  • Health assessment questionnaire disability index [Срок оценки: 3 months]
  • Psoriasis Area and Severity Index [Срок оценки: 3 months]

Критерии участия

Критерии включения

  • This study will include 60 adult Psoriatic arthritis patients >18 years old, fulfilling the (CASPAR) classification criteria of Psoriatic arthritis and have an inadequate response to methotrexate therapy for at least 3 months.
  • Psoriatic arthritis patients with peripheral musculoskeletal domains (peripheral arthritis, dactylitis and enthesitis) as well as skin and nail domains

Критерии исключения

  • Patients who received previous biologic agents or Janus kinase inhibitors.
  • Patients with axial and ocular involvement.
  • Current or recent serious infection including tuberculosis or hepatitis B/C .
  • Current or past history of malignancy (within five year).
  • Pregnant or breastfeeding women or women planning pregnancy during the study period .
  • Severe uncontrolled comorbidities such as heart failure, severe liver disease, or chronic kidney disease (eGFR <30 mL/min/1.73m²) .

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
Двойное слепое
Основная цель
Лечение

Центры проведения

Египет · 1 центр
  • Tanta University — Tanta

Идентификаторы

NCT: NCT07398651 · 36265MD4108/12 / 25

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗