Actively Recruiting

Phase 4
Age: 18Years - 45Years
All Genders
NCT06575179

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

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-45 years.
  • American Society of Anesthesiologists (ASA) grade I - II.
  • Patients undergoing elective laparoscopic cholecystectomy.
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Fujian Provincial Hospital

Fuzhou, Fujian, China, 350001

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here