Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-25 @ 1:14 AM
Ignite Modification Date:
2025-12-25 @ 11:24 PM
NCT ID:
NCT05126693
Group ID:
EG000
Title:
Intervention Group
Description:
The children in the intervention group will receive BoNT injections in the medial gastrocnemius and/or the semitendinosus muscle(s). As part of the standard treatment approach of the CP Reference Centre of the University Hospitals Leuven, the injections are followed by a period of bilateral stretching casts if indicated (below the knee walking casts and removable knee extension casts when necessary).
All children will then undergo an intensive physical therapy program lasting 8-10 weeks. This post-BoNT therapy phase is guided by individualized treatment goals, which are established based on baseline assessments. These goals are determined during a multidisciplinary meeting with the treating physician, held prior to the BoNT injections.
Thus, the intervention consists of BoNT treatment combined with an 8-10 week period of intensive physical therapy tailored to each child's specific therapeutic needs.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
25
Other Number Affected:
0
Other Number At Risk:
25
Study:
NCT05126693
Results Section:
NCT05126693
Adverse Events Module:
NCT05126693