Post Surgical Multimodal Analgesia With Oral Strong Opioids
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: Multimodal analgesia with oral strong opioids.
- Кому может быть актуально
- Состояния в реестре: Orthopedic Procedures, Arthroplasty, Fracture Fixation. 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
- Тайвань
- 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
Study on the Clinical Effectiveness of Oral Strong Opioids for Common Orthopedic Surgeries Following Multimodal Analgesia
Обзор
This is a prospective observational case study, focusing on the clinical effectiveness of oral strong opioids for pain management following common orthopedic surgeries.The study aims to evaluate the effectiveness of multimodal analgesia with oral strong opioids, reduce common opioid-related side effects, and improve patient compliance and satisfaction.
Вмешательства
- Препарат Multimodal analgesia with oral strong opioids
Physician's choice of post-surgical multimodal analgesia with an oral strong opioid as the backbone analgesics
Первичные конечные точки
- Change in pain scores from baseline [Срок оценки: Twice daily during hospitalization (approximately within 1 week), at the first return 1 day visit and at 3 months after surgery]
Вторичные конечные точки (4)
- Occurence of adverse events [Срок оценки: During hospitalization (approximately within 1 week)]
- Compliance of oral strong opioids [Срок оценки: During hospitalization (approximately within 1 week)]
- Physician's global impression - improvement scale(CGI-I) [Срок оценки: During hospitalization (approximately within 1 week), at the first return 1 day visit and at 3 months after surgery]
- Satisfation of the pain control as per patients' report outcome [Срок оценки: End of hospitalization (approximately 1 week after surgery)]
Критерии участия
Критерии включения
- Aged 18 or older
- Must undergo one of the following treatments:
(1) Fracture of upper or lower limbs or pelvis requiring internal fixation surgery (2) Spinal fusion surgery (3) Joint replacement surgery 3. Requiring multimodal analgesics for postoperative pain control, with oral strong opioids as the primary opioid analgesic, as assessed by his/her physician.
4\. Voluntarily sign the informed consent form and agree to the collection of clinical questionnaires and medical-related information for this study.
Критерии исключения
- Patients who have not received any or have only received oral potent opioids for no more than 1 day during the postoperative hospitalization period (including those known to be intolerant or allergic to opioid medications).
- Patients who have received or are expected to use long-acting opioid injections within 7 days before surgery or during the postoperative hospitalization period.
- Patients who use patient-controlled analgesics for pain control after surgery.
- Patients with a history of substance abuse or who require continuous treatment with other opioid receptor agonists or antagonists (such as naloxone or methadone).
- Patients with a history of mental illness who continue to require medication control from 28 days before surgery and until discharge.
- Other cases deemed ineligible by the study investigator.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Только случаи
Центры проведения
Тайвань · 1 центр
- TriService General Hospital — Taipei
Идентификаторы
NCT: NCT06554457 · ORORA24