Clinical trial

Opioid-free Anesthesia, Optimization of Anesthesia - Comparison of the Effectiveness of Analgesic and Antiemetic Effects in Patients After Bariatric Surgery

Name
1072.6120.135.2023
Description
Total intravenous general anesthesia and combined general anesthesia are recognized methods used during anesthesia. They allow you to effectively control pain and reduce the number of complications associated with taking large doses of opioid drugs. It should be emphasized that both methods of anesthesia are currently approved for use in routine anesthetic practice, and only the experience, knowledge and preferences of the anesthesiologist determine which technique will be used in a given patient. Both techniques are used in everyday anesthetic practice, but there is no conclusive scientific data confirming the superiority of either method in patients undergoing bariatric surgery, therefore currently only the individual experience, knowledge and preferences of the anesthesiologist determines which technique will be used in a given patient.
Trial arms
Trial start
2024-03-14
Estimated PCD
2025-12-31
Trial end
2025-12-31
Status
Recruiting
Treatment
Intubation
Comparing videao laryngospy with traditional laryngoscopy
Arms:
Conventional, Video-Laryngoscope
TIVA versus Inhalation
comparing TIVA with genera anesthesia with inhalation agent
Arms:
Inhalation agent, TIVA
Size
200
Primary endpoint
compare the effectiveness of analgesia
2 days
determine whether modern technologies such as videolaryngoscopy shorten intubation time.
1 day
Eligibility criteria
Inclusion Criteria: * Patients over 18 years who underwent laparoscopic bariatric surgery Exclusion Criteria: Patients with a history of allergic reactions to drugs Patients with a history of drug addiction Patients with chronic pain who require analgesics History of hospitalization for psychiatric disorders Preoperative pulse oximetry (SpO2) \< 95 % bradycardia (HR\<50bpm), hypotension, atrioventricular block, intraventricular or sinus block Blood clotting disorders Pregnant/lactating women Cognitive impairment Unable to read consent
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'The study group will be male and female patients, ASA II or III, over 18 years of age and under 75 years of age. Each patient will undergo abdominal (bariatric) surgery.', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['INVESTIGATOR']}}, 'enrollmentInfo': {'count': 200, 'type': 'ESTIMATED'}}
Updated at
2024-04-29

1 organization

1 product

3 indications

Indication
Analgesics
Indication
Opioid
Indication
Anesthesia