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Postoperative Temperature Monitoring In Brain Trauma

A Muti-centre Prospective Observational Study on Postoperative Temperature Monitoring In Patients With Brain Trauma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03068143
Acronym
PTMIBT
Enrollment
150
Registered
2017-03-01
Start date
2017-03-31
Completion date
2018-02-28
Last updated
2017-03-01

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

Conditions

Body Temperature Changes, Brain Injuries, Traumatic

Brief summary

This prospective observational study is designed to investigate the relationship between brain temperature, axillary temperature, rectal temperature, and bladder temperature of postoperative patients with brain trauma, and the relationship between brain temperature and prognosis. This study is conducted based on the following important assumptions. First, brain temperature of postoperative patients with brain trauma should be higher than the axillary temperature, rectal temperature and bladder temperature. Second, the consistency of brain temperature and bladder temperature is better than the consistency of brain temperature and axillary temperature, as well as that of brain temperature and rectal temperature. Third, brain temperature can help clinicians to predict the prognosis of patients with brain trauma. Therefore, brain temperature monitoring is significant in postoperative intensive care and treatment of patients with brain trauma.

Interventions

None listed

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Clinical or radiological diagnosis is brain trauma; * The patient has surgical indications, and the patient or his/her family are willing to undergo operation including brain temperature monitoring probe implantation; * Informed consent is obtained from the patient's family.

Exclusion criteria

* At the time of admission there are serious systemic diseases, including severe infections, immune system diseases, blood system diseases, infectious diseases, severe liver and kidney dysfunction, malignant tumors, etc; * Pregnant or lactating women; * There are other brain tumors or cerebrovascular disease in the brain at the same time; * There is a history of drug or alcohol abuse; * Within 3 months before admission, live vaccines were inoculated.

Design outcomes

Primary

MeasureTime frameDescription
Change of Brain TemperatureChange from Baseline Brain Temperature at 1 week
Change of Axillary TemperatureChange from Baseline Axillary Temperature at 1 week
Change of Rectal TemperatureChange from Baseline Rectal Temperature at 1 week
Change of Bladder TemperatureChange from Baseline Bladder Temperature at 1 week
Glasgow Outcome Scale1 monthAn objective assessment of the recovery of patients with brain trauma

Countries

China

Contacts

Primary ContactGuoyi Gao, Dr.
guoyigao@gmail.com+86-021-68383709

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026