Actively Recruiting
Early Body Temperature Targets and Relationship With Prognosis in Patients With Heat Stroke
Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2024-09-20
100
Participants Needed
6
Research Sites
21 weeks
Total Duration
On this page
Sponsors
S
Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead Sponsor
Y
Yiwu Central Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting an observational study to explore the best target body temperatures during the first 24 hours after heat stroke and how these temperatures relate to patient outcomes. The study aims to find optimal body temperatures at specific times after heat stroke, the best body temperature to stop cooling, and how the amount and speed of ice saline infusion affect cooling. This research is sponsored by the Second Affiliated Hospital, School of Medicine, Zhejiang University. Participants in this study are patients with heat stroke who come to the emergency department at the study site. Patients will receive standard cooling treatments and organ function support as part of their usual care. The study does not involve experimental treatments but observes how current practices affect body temperature and outcomes. During the study, researchers will monitor patients’ body temperatures at various times and track outcomes such as mortality and organ damage up to 90 days after heat stroke. Additional measures include the need for continuous renal replacement therapy, length of stay in the intensive care unit, and total hospital stay. Participants’ progress will be observed through routine clinical care without additional interventions specific to the study.
CONDITIONS
Brief Title
Early Body Temperature Targets and Relationship With Prognosis in Patients With Heat Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Diagnosed with heat stroke
- Provided informed consent by patient or family member
You will not qualify if you...
- Requires immediate cardiopulmonary resuscitation
- Transferred from another hospital
- Has severe underlying organ insufficiency
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 90 days
Participants who undergo routine care are observed to assess early body temperature targets and their relationship with prognosis.
Trial Site Locations
Total: 6 locations
1
Yiwu Central Hospital
Yiwu, Zhejiang, China
Actively Recruiting
2
Dongyang People's Hospital
Dongyang, China
Actively Recruiting
3
The Second Affiliated Hospital of Zhejiang University School of Medicine
Hangzhou, China, 310000
Actively Recruiting
4
Jinhua Municipal Central Hospital
Jinhua, China
Actively Recruiting
5
Jinhua People's Hospital
Jinhua, China
Actively Recruiting
6
Lanxi People's Hospital
Lanxi, China
Actively Recruiting
Research Team
X
Xiuqin Feng
L
Lan Chen
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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