Design and implementation of a national multicenter registry for pediatric patients with CNS lesions treated with robotic radiosurgery

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00016973

Enrollment

200

Registered

2019-03-18

Start date

2019-06-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

brain tumors Q28.2 D33 C71 C72 D33.4

Interventions

Group 1: The CyberKnife Registry is an observational study, intending to register all pediatric patients who have been treated with Cyberknife radiosurgery for lesions in the central nervous system. P

Eligibility

Sex/Gender

All

Age

0 Years to 17 Years

Inclusion criteria

Inclusion criteria: age < 18, diagnosis of CNS lesion, interdisciplinary consent for radiosurgical intervention, possibility of consecutive follow up controls, consent form signed by both parents (and child depending on his/her age)

Exclusion criteria

Exclusion criteria: age of 18 or older, pregnancy, breast feeding

Design outcomes

Primary

Measure	Time frame
Primary endpoints are complete remission and recidive at 1 and 2 years of follow-up	—

Secondary

Measure	Time frame
Secondary end points are side effects, radiation toxicity and long-term effects	—

Countries

Germany

Contacts

Public ContactLaura-Nanna Lohkamp

Charité-Universitätsmedizin Berlin, Klinik für Neurochirurgie

Laura-Nanna.Lohkamp@charite.de+14379952406 oder +491716433518

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026