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
144 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
The goal of this observational study is to explore the optimal target body temperature in first 24 hours and the relationship between body temperature and adverse outcomes of heat stroke. The main questions it aims to answer are: * the optimal target body temperature at 0.5 h, 2 h, and the lowest body temperature of heat stroke. * the best body temperature at the cutting point of stop cooling. * The relationship between the volume and speed of ice saline infusion and the cooling effect.
CONDITIONS
Official 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 or older
- Diagnosed with heat stroke
- Informed consent given by patient or family member
You will not qualify if you...
- Require immediate cardiopulmonary resuscitation
- Transferred from another hospital
- Have severe underlying organ insufficiency
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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
CONTACT
L
Lan Chen
CONTACT
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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