跳至主要内容
临床试验/2024-514852-34-01
2024-514852-34-01招募中3 期

Prospective pilot study of L-dopa treatment in patients with a neurodevelopmental disorder linked to a pathogenic variant of the CTNNB1 gene

Centre Hospitalier Universitaire De Montpellier1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2025年8月14日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
7
试验地点
1
主要终点
GMFM-88 motor score before treatment (Day 1) and at 6 months

研究概览

简要总结

Evaluate the effect of treatment on patients' motor skills by assessing their motor skills before and after treatment with the 88-item Gross Motor Function Measure (GMFM-88).

研究设计

分配方式
Not Applicable
主要目的
Assessment Of Physical And Cognitive Abilities
盲法
None

入排标准

年龄范围
0 years 至 17 years(0-17 Years)
接受健康志愿者

入选标准

  • Ages 1 to 15 inclusive
  • Carrier of a pathogenic variant of CTNNB1.

排除标准

  • Contraindication to treatment with L-dopa and carbidopa or one of its excipients
  • Current treatment with L-dopa, dopamine agonist or dopamine blocker,
  • Failure to obtain informed consent signed by both parents or legal guardians, and to obtain the child's assent if possible.
  • Patient not enrolled in or benefiting from a social security scheme
  • Person participating in another research project with an exclusion period still in progress

结局指标

主要结局

GMFM-88 motor score before treatment (Day 1) and at 6 months

GMFM-88 motor score before treatment (Day 1) and at 6 months

次要结局

  • GMFM-88 motor score before treatment (Day 1) and at 12 months
  • Changes in language/development/cognition assessment scores (Bayley III, WPPSI, WISC, Vineland), before treatment and at 1 year after treatment
  • Changes in quality-of-life scores (Caregiver Priorities & Child Health Index of Life with Disabilities (CP-CHILD), Clinical Global Impression of severity scale (CGI)) before treatment, at 6 months and at 1 year after initiation of treatment
  • Tolerance assessment (number and severity of adverse events, clinical follow-up, clinical, neurological and osteoarticular examination, patient logbook).
  • GMFM-88 motor score between 6 and 12 months of treatment

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Agathe ROUBERTIE

Scientific

Centre Hospitalier Universitaire De Montpellier

研究点 (1)

Loading locations...

相似试验