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.

our participation in this research will be kept completely confidential. The only person aware of your participation in the research will be the project director. Clinical information, including the information you provide to your doctor, will be kept confidential. However, inspectors from the relevant authorities may be required to review your records to ensure that the research is conducted in accordance with applicable laws and health authorities regulations. The information in your records will only be used for the purpose of this research and for publications following this research. In all cases, your identity will be kept confidential. In all cases, your identity will not be used for other purposes or disclosed to third parties. You will not be charged for your examinations and other procedures. I have read and heard the information above, which must be given to the volunteer before starting the research. I have read all the explanations in the Informed Consent Form. I have received written and oral explanations regarding the research, the subject and purpose of which are stated above, from the physician/researcher whose name is listed below. I have asked the researcher all the questions that came to mind, and I have fully understood all the explanations given to me in writing and orally. I was given sufficient time to decide whether or not I wanted to participate in the study. I understand that I am participating in the research voluntarily, that I can withdraw from the research at any time with or without justification, and that I may be excluded from the research by the researcher regardless of my wishes. I agree to participate in the said research of my own free will, without any pressure or coercion, and I authorize the researcher to review, transfer, and process my medical information. I accept the invitation to participate in this research with great willingness and without any coercion or pressure.

Inclusion Criteria:

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

Exclusion Criteria:

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

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