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Clinical Analysis of Early Hormones Between Patients With Traumatic Brain Injury and Cerebral Hemorrhage

Clinical Analysis of the Hormone Between Patients With Moderate and Severe Traumatic Brain Injury and Cerebral Hemorrhage

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06221215
Enrollment
100
Registered
2024-01-24
Start date
2023-10-01
Completion date
2024-12-31
Last updated
2024-01-24

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

Conditions

Brain Injury Traumatic Diffuse With Loss of Consciousness

Keywords

Traumatic brain injury, Cerebral hemorrhage, hormone, trauma

Brief summary

Our understanding of neurosecretory dysfunction after TBI is still insufficient, and the number of patients with neuroendocrine dysfunction caused by craniocerebral trauma may be underestimated, especially the neuroendocrine changes related to HPA axis in the early stage after craniocerebral trauma. Moreover, there are few and fragmentary literature data on the benefits of hormone replacement therapy in patients with neuroendocrine disorders after traumatic brain injury. This requires more studies to further determine the characteristics of pituitary function or hormone disorders in the early stage after traumatic brain injury, which makes it necessary for us to further study the neuroendocrine dysfunction (hormone disorder) in the early stage after craniocerebral injury. To explore the relationship between craniocerebral injury and early hormone disorder by measuring the changes of early hormone levels in patients with TBI is of great significance for the early detection of related complications after craniocerebral injury and the evaluation of the prognosis of patients with craniocerebral injury, and can provide a new diagnosis and treatment plan for early intervention of related complications after TBI.

Interventions

PROCEDUREtrauma

The main purpose of this study is to observe whether the early hormone changes and trends in the two groups of patients with or without trauma.

Sponsors

General Hospital of Ningxia Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years old. 2. The patient was clearly diagnosed as craniocerebral injury. 3. The Glasgow score on admission was 3-12 (moderate and severe). 4. It has complete preclinical data.

Exclusion criteria

1. Complicated with other severe visceral injuries or severe systemic fractures. 2. Suffered from craniocerebral tumors, endocrine diseases, cardiovascular diseases, depression, sleep and mental disorders. 3. In the past month, there are people who receive immune and hormone therapy. 4. Women during pregnancy and lactation. 5. Where there is a logical or common sense error in the data entered. 6. The lack of too much clinical data related to this study.

Design outcomes

Primary

MeasureTime frameDescription
Change of GH1st, 7th and 14th day.The levels of related hormones (growth hormone) were measured in patients with TBI.
Change of pituitary prolactin1st, 7th and 14th day.The levels of related hormones (pituitary prolactin) were measured in patients with TBI.
Change of ACTH1st, 7th and 14th day.The levels of related hormones ( ACTH) were measured in patients with TBI.
Change of cortisol1st, 7th and 14th day.The levels of related hormones (cortisol) were measured in patients with TBI.
Change of FSH1st, 7th and 14th day.The levels of related hormones (FSH) were measured in patients with TBI.
Change of thyroid hormone1st, 7th and 14th day.The levels of related hormones (thyroid hormone) were measured in patients with TBI.

Countries

China

Contacts

Primary ContactZhanfeng Niu, Doctor
niuzfeng228626@163.com+8613995297581

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026