Actively Recruiting
A Study to Explore the Role and Impact of Wearable Smart Devices in Perioperative NSCLC Patients
Led by The First Affiliated Hospital of Guangzhou Medical University · Updated on 2024-06-28
300
Participants Needed
1
Research Sites
159 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The trial was designed as a single-center non-interventional prospective observational study to explore the role and impact of wearable smart devices in perioperative NSCLC patients.
CONDITIONS
Official Title
A Study to Explore the Role and Impact of Wearable Smart Devices in Perioperative NSCLC Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must voluntarily consent to participate and be able to sign an informed consent form.
- Participants must be over 18 years old.
- Participants must have undergone pulmonary resection surgery with postoperative pathological confirmation of primary lung cancer.
You will not qualify if you...
- Patients who refuse to participate.
- Inability to wear wearable smart monitoring devices.
- Pathological report indicating exclusion of non-small cell lung cancer (NSCLC).
- History of previous secondary lung cancer surgery.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Thoracic Surgery and Oncology, The First Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, China
Actively Recruiting
Research Team
J
Jianxing He, M.D
CONTACT
W
Wenhua Liang, M.D
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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