Clinical Outcomes of Intubation Techniques in Anesthesia

ConditionLaparoscopic

Trial statusNot yet recruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

Age18+

SponsorAmasya University

About this trial

Before surgery, patients will be evaluated by an anesthesiologist at the anesthesia clinic and informed in detail about the study. Patients who do not wish to participate in the study will absolutely not be included, and this will not affect the patients' treatment process in any way. The anesthesia method to be applied to patients who agree to participate in the study will not differ from routine anesthesia application. In other words, no additional medication, procedure, or different anesthesia method will be applied to patients within the scope of the study. After the surgery is completed, patients will be monitored in the recovery room and during their hospital stay. During this monitoring, it will be observed and recorded whether patients have complaints such as sore throat, cough, or hoarseness.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients over 18 years of age ASA 1-2-3 patients undergoing elective laparoscopic cholecystectomy surgery Patients who agreed to participate in the study

Disqualifiers

Patients for whom difficult intubation is considered Patients with neurological disorders Patients with mental retardation Patients who refused to participate in the study.

Trial population

This study aims to determine the incidence of postoperative cough and sore throat using endotracheal intubation techniques in laparoscopic cholecystectomy surgeries.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

165 Participants

are grouped into 3 trial groups

Group A: group laryngoscopy

Group B: group videolaryngoscopy

Group C: group fiberoptic bronchoscopy

Trial outcomes

Primary outcomes

sore throat

Postoperative sore throat will be defined as persistent sore throat and its severity will be assessed using a visual analog scale (VAS) rated from 1 to 10.

Time frame

1 day

primaty

The primary objective of the study is to evaluate the intubation success rates of three different intubation techniques.

Time frame

1 day

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Amasya University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: