A Prospective Cohort Study of ITB Treatment for HSP

Официальное название

Intrathecal Baclofen for the Management of Hereditary Spastic Paraparesis: a Prospective Cohort Study

Обзор

The investigators conduct a prospective cohort study to explore the treatment effectiveness of continuous infusion of intrathecal baclofen (ITB) for hereditary spastic paraplegia (HSP) in China, delve into the optimal timing for starting treatment, and investigate the response differences among different subtypes. The ultimate goal is to provide clinical evidence and guidance for the application of ITB in treating HSP in China, as well as improve the life expectancy and quality of life for HSP patients. The main questions it aims to answer are: 1. Changes in gait and motor function, as well as spasticity levels, compared to pre-surgery and control group after ITB surgery. 2. Changes in quality of life, pain, psychological and emotional status, and cognition compared to pre-surgery and control group after ITB surgery. 3. Complications following ITB surgery. 4. Impact of ITB surgery on the occurrence and progression of skeletal deformities. 5. Subgroup analysis: comparing surgical outcomes between different genotypes and between simple versus complex types. 6. Determine the optimal timing for ITB intervention.

Подробное описание

Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and weakness of the lower limbs due to retrograde axonal degeneration of the corticospinal tract. Baclofen is a selective GABA-B receptor agonist and is commonly used for the treatment of spasticity. Baclofen can be administered orally or intrathecally by the surgical implantation of a specialized pump. Intrathecal baclofen (ITB) is significantly more potent for the treatment of spasticity than the oral form. The goal of this clinical trial is to explore the efficacy and safety of ITB in the treatment of HSP patients. This study is prospective, open-label, single center, and this trial will last for 3 years. A total of 50 patients will participate. Twenty-five patients who will receive ITB and the other 25 control patients will receive oral baclofen. Patients with HSP aged 14 to 70 years, with a Modified Ashworth Scale score of ≥3 in ≥2 joints of lower limb, will be recruited. Patients who do not agree to undergo ITB and/or those who have an inadequate response during intrathecal baclofen test will receive oral baclofen therapy and undergo natural history observation. Professional clinical evaluations are conducted regularly for both groups.

Первичные конечные точки

• Six-Minute Walk Test(6-MWT) [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Step length [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• walking speed [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• knee flexion angle [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Modified Ashworth Scale(MAS) [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Range of Motion (ROM) of Joints [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]

Вторичные конечные точки (12)

• Patient Global Impression of Change (PGIC) scale [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Oswestry Disability Index (ODI) [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Numeric Rating Scale (NRS) [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• MMSE score [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• MoCA score [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• SDS [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• SAS [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• SPRS score [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Complications [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• GMFM-88 [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• GAS [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]
• Foot deformity molding [Срок оценки: From the end of treatment to observations at 6 months, 12months, 18months, 24months, 30months, and 36months respectively]

Критерии участия

Критерии включения

• Patients meet the clinical and genetic diagnostic criteria of hereditary spastic paraplegia (HSP);
• Age: 14 to 70 years old
• Modified Ashworth Score for lower limbs: ≥2 joints with muscle tone ≥grade 3
• Patients are willing to participate in clinical trials and able to understand and comply with the research program

Критерии исключения

• Patients are allergic to the baclofen
• Other neurological diseases likely affecting the evaluation of study treatment
• Other medical conditions such as: heart disease, tumor, blood disease, liver disease, kidney disease, etc. in the past 1 year
• Pregnancy or lactating women or subjects who are unable to use appropriate contraception during the trial
• Participating in another study drug trial and used the investigational drug in the past 30 days
• Subjects have poor compliance or other factors that are not suitable for participating in the clinical trial

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Когортное

Центры проведения

Китай · 1 центр

• Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Med — Шанхай

Идентификаторы

NCT: NCT06844734 · 2024-KY-305(K)

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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