Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
76 participants
INTERVENTIONAL
2025-03-15
2025-04-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Different Fresh Gas Flows on Carboxyhemoglobin Levels and Postoperative Patient Outcomes in Pediatric Cardiovascular Surgery
NCT06097806
Does Low Flow Anesthesia Reduce Postanaesthetic Emergence Agitation?
NCT03862391
Low-Flow Desflurane Anesthesia and Its Effects on BIS and Postoperative Cognitive Functions
NCT07212543
Comparison of Minimum Flow and Low Flow Desflurane Anesthesia in Robotic Assisted Laparoscopic Abdominal Surgery
NCT06520943
Low-Flow Anesthesia and Open-Heart Surgery
NCT07040735
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SCREENING
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
low flow anesthesia
Maintenance of anaesthesia with low-flow anaesthesia
Sevoflurane (Volatile Anesthetic)
Both groups will be given sevoflurane and one group will be given low current anesthesia and the other group will be given medium flow anesthesia.
low- medium flow anesthetic machine
The study aims to compare the effects of low and normal flow sevoflurane anesthesia on the frontal QRS-T angle and cerebral oxygenation in laparoscopic cholecystectomy surgery.
Medium Flow Anesthesia
Maintenance of anaesthesia with medium-flow anaesthesia
Sevoflurane (Volatile Anesthetic)
Both groups will be given sevoflurane and one group will be given low current anesthesia and the other group will be given medium flow anesthesia.
low- medium flow anesthetic machine
The study aims to compare the effects of low and normal flow sevoflurane anesthesia on the frontal QRS-T angle and cerebral oxygenation in laparoscopic cholecystectomy surgery.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Sevoflurane (Volatile Anesthetic)
Both groups will be given sevoflurane and one group will be given low current anesthesia and the other group will be given medium flow anesthesia.
low- medium flow anesthetic machine
The study aims to compare the effects of low and normal flow sevoflurane anesthesia on the frontal QRS-T angle and cerebral oxygenation in laparoscopic cholecystectomy surgery.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* between the ages of 18-70
* who are planned for laparoscopic cholecystectomy
Exclusion Criteria
* Pregnant and breastfeeding patients
* Morbidly obese patients (Body mass index over 40)
* Patients with uncontrolled diabetes mellitus, with serious cardiovascular, pulmonary, renal, hepatic disease, obstructive sleep apnea, with electrolyte imbalance- Those with a history of alcohol or drug abuse, with perioperative hemodynamic instability
* Patients using drugs known to prolong myocardial repolarization
* inability to increase SPO2 above 95 despite necessary intervention
17 Years
70 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Umraniye Education and Research Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Senay Goksu
specialist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
SENAY GOKSU, MD
Role: PRINCIPAL_INVESTIGATOR
UMRANIYE E R HOSPITAL
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Umraniye Education and research hospital
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
LFATUGCE
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.