Actively Recruiting
Impact of Propofol-Based Total Intravenous Anesthesia Versus Anesthesia With Sevoflurane on Long-term Outcomes With Patients Undergoing Elective Excision of Primary Liver Tumors
Led by Kaohsiung Medical University Chung-Ho Memorial Hospital · Updated on 2022-11-30
500
Participants Needed
1
Research Sites
257 weeks
Total Duration
On this page
Sponsors
K
Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead Sponsor
T
Tri-Service General Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a two-arm, parallel-group randomized clinical trial. Routine perioperative care would be performed in volunteers with primary Hepatocellular carcinoma. The study will enroll approximately 500 volunteers to compare the progression-free or overall survival in patients undergoing elective partial hepatectomy for primary liver tumors between propofol and sevoflurane for the maintenance of anesthesia.
CONDITIONS
Official Title
Impact of Propofol-Based Total Intravenous Anesthesia Versus Anesthesia With Sevoflurane on Long-term Outcomes With Patients Undergoing Elective Excision of Primary Liver Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 20 and 80 years
- ASA physical status class I to III
- Scheduled for partial hepatectomy for hepatocellular carcinoma under general anesthesia
You will not qualify if you...
- Severe mental disorder
- Pregnant or lactating women
- Morbid obesity
- Allergy to any drugs used in the study
- Recurrent tumor or repeat surgery
- Biopsy cases
- Incomplete data collection before surgery
- Planned palliative treatment after surgery
- Treatment for other malignancies at the same time
- Combined use of propofol and inhalation anesthesia or other anesthetics such as ketamine or dexmedetomidine
- Diagnosed with benign liver tumor
- Emergency surgery
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Kaohsiung Medical University Chung-Ho Memorial Hospital
Kaohsiung City, Taiwan
Actively Recruiting
Research Team
G
Guan-Yu Chen, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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