Actively Recruiting
Dexmedetomidine Reduces Sevoflurane MAC-BAR During Pneumoperitoneum
Led by Fujian Provincial Hospital · Updated on 2024-10-01
90
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial aims to learn the impact of dexmedetomidine on the minimum alveolar concentration blunting the adrenergic response (MAC-BAR) of sevoflurane to carbon dioxide pneumoperitoneum in patients undergoing laparoscopic cholecystectomy. It will also learn about the effect of dexmedetomidine on hemodynamic parameters. The main questions are: * Does dexmedetomidine reduce the MAC-BAR of sevoflurane required to suppress the sympathetic response to carbon dioxide pneumoperitoneum? * Would dexmedetomidine administration dose-dependently reduce the minimum alveolar concentration blunting the adrenergic response of sevoflurane required to suppress the sympathetic response to carbon dioxide pneumoperitoneum? Researchers will compare low-dose dexmedetomidine to high-dose dexmedetomidine to see if dexmedetomidine works to treat postoperative negative behavior change and emergence delirium. Participants will: * Take intravenous dexmedetomidine or 0.9% saline (a look-alike substance that contains no drug) * Study drug infusions were initiated 15 minutes prior to anesthesia induction, allowing a minimum of 30 minutes to elapse before surgical incision to achieve steady-state plasma and brain concentrations.
CONDITIONS
Official Title
Dexmedetomidine Reduces Sevoflurane MAC-BAR During Pneumoperitoneum
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-45 years.
- American Society of Anesthesiologists (ASA) grade I - II.
- Patients undergoing elective laparoscopic cholecystectomy.
You will not qualify if you...
- Inability to provide informed consent.
- History of chronic pain or substance abuse.
- Pregnancy.
- Body mass index (BMI) 60 30 kg/m2.
- Known allergies to the study medications.
- Intake of medications within the last 72 hours that may interfere with MAC-BAR determination.
- Any other condition deemed exclusionary by the investigators.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Fujian Provincial Hospital
Fuzhou, Fujian, China, 350001
Actively Recruiting
Research Team
Y
Yusheng Yao, MD&PhD
CONTACT
S
Sisi Chen, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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