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Prevalence of growth hormone deficiency in adults after stroke

Prevalence of growth hormone deficiency in adults after stroke

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060854
Enrollment
Unknown
Registered
2022-06-12
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Adult Growth Hormone Deficiency

Interventions

1:Cross-sectional survey

Sponsors

Tai 'an City Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 65; 2. Stroke patients: Acute focal or comprehensive clinical symptom, neurologic deficits and duration of clinical symptoms and signs of the neurologic deficits for more than 24 hours, and to rule out other non vascular causes (such as primary brain tumor, subdural hematoma, brain metastases, brain injury after seizures, paralysis, etc.) caused by brain dysfunction, Skull MRI or CT confirmed focal hemorrhage or infarction [1, 2]. 3. When subjects signed the informed consent and entered the screening period, the time between stroke occurrence was more than 1 week and less than 26 weeks; The subject is willing and able to cooperate with the scheduled visit, treatment plan, laboratory examination and other test procedures, and sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Disturbance of consciousness during screening, including drowsiness, lethargy, coma, confusion, and delirium. 2. Pregnancy: For women with fertility potential, a negative pregnancy urine test is required. 3. Hba1c > 9.0% at screening. 4. Renal insufficiency (serum creatinine > 3.0 mg/dL) or end-stage renal disease. Kidney replacement therapy is required. Systolic blood pressure < 90mmHg and/or diastolic blood pressure < 50mmHg. 6. Ecg abnormalities of clinical significance that are considered inappropriate for inclusion in this study. 7. Not suitable for venipuncture. 8. Congestive heart failure, New York Heart Association (NYHA) Class III or IV. 9. History of seizures. 10. History of pheochromocytoma and/or islet tumor. 11. History of glycogen accumulation. 12. Participated in clinical trials of any drug or medical device within 3 months prior to screening (except those who signed informed consent only and did not receive any drug or device intervention) 13. Used growth hormone therapy in the past one year; Other reasons the researchers say need to be ruled out.

Design outcomes

Primary

MeasureTime frame
Blood routine examination;Growth Hormone;IGF-1;Thyroid function five;Blood cortisol and ACTH ;Blood fat;Serum homocysteine;CRP;Fasting blood-glucose;Total glycaemic hemoglobin;Head CT and/or MRI;National Institute of Health stroke scale;Montreal Cognitive Assessment;Modified Rankin Scale, mRS;Self—Rating Anxiety Scale;Self-Rating Depresion Seale;Insulin Tolerance Test;

Countries

China

Contacts

Public ContactZuncheng Zheng
zxyyzhengzuncheng@126.com+86 13375388062

Outcome results

None listed

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