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Efficacy and Safety of Growth Hormone Therapy for Growth Hormone Deficiency Following Treatment of Paediatric Intracranial Tumours: An Observational Study

Efficacy and Safety of Growth Hormone Therapy for Growth Hormone Deficiency Following Treatment of Paediatric Intracranial Tumours: An Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119460
Enrollment
Unknown
Registered
2026-02-27
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Growth Hormone Deficiency Following Treatment of Intracranial Tumours in Paediatric Patients

Interventions

Growth hormone treatment group:None
No growth hormone treatment group:None

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: (1).Children who meet all of the following criteria: (1) Histologically confirmed survivors of intracranial tumours, including craniopharyngioma, germ cell tumours, gliomas, etc. (2) Age at tumour diagnosis < 18 years. (3) Completion of intracranial tumour treatment, defined as the last optimal debulking surgery or last radiotherapy session. (4) Whether or not surgery was performed. (5) Diagnosed with growth hormone deficiency. (6) Currently undergoing GH therapy for less than one year at study initiation, or requiring growth hormone therapy at present. (7) Complete key data including event-free survival rates and height measurements at baseline and follow-up periods in retrospective records.

Exclusion criteria

Exclusion criteria: Meeting any one of the following criteria: (1) Non-intracranial tumour. (2) Renal failure. (3) Growth hormone deficiency unrelated to intracranial tumours and/or their treatment. (4) Patients lacking detailed preoperative/postoperative hospital records. (5) Cancer susceptibility syndromes. (6) Other circumstances deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Event-free survival rate;

Secondary

MeasureTime frame
Incidence of adverse events;?Ht SDS;

Countries

China

Contacts

Public ContactWang Zhujun

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

wangzhujun2009@126.com+86 27 8572 6114

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026