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To investigate the endocrine and metabolic characteristics of children with different types of sellar lesions and to refine multiple pituitary hormone replacement strategies

To investigate the endocrine and metabolic characteristics of children with different types of sellar lesions and to refine multiple pituitary hormone replacement strategies

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095686
Enrollment
Unknown
Registered
2025-01-10
Start date
2025-01-13
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Sellar region lesions

Interventions

Growth hormone treatment group (retrospective section):None
Non growth hormone treatment group (retrospective section):None
Observation group (prospective section):None

Sponsors

Shanghai Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 18 Years

Inclusion criteria

Inclusion criteria: a. Definitive diagnosis of sellar region lesions (as agreed upon by multidisciplinary consensus including neurosurgery, radiology, oncology, and endocrinology) b. Imaging or pathological evidence is available c. Patients have undergone or are undergoing surgical, radiotherapeutic, and/or chemotherapeutic interventions d. Comprehensive endocrine evaluations are documented e. Baseline metabolic assessment data are available f. Robust follow-up data are available g. Patients have received or are currently receiving endocrine hormone therapy h. Detailed and standardized electronic medical records or convertible forms are maintained;

Exclusion criteria

Exclusion criteria: a. The patient's neuroendocrine system exhibited severe impairment, and the caregiver was unable to provide adequate support. b. The lesions were widespread, with the sellar region not being the primary affected area. c. Metastatic tumors were present in the sellar region. d. Any other conditions that the investigator deemed unsuitable for trial inclusion.

Design outcomes

Primary

MeasureTime frame
HtSDS;Tumor-free survival;

Secondary

MeasureTime frame
Pituitary hormone levels (including thyroid function, adrenal function, vasopressin, sex hormones, etc.);Lipid metabolism levels;Assessment of Sexual development;Quality of Life;

Countries

China

Contacts

Public ContactSheng Guo

Shanghai Children's Hospital

guosheng@shchildren.com.cn+86 21 52976355

Outcome results

None listed

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