Clinical Outcomes of Intubation Techniques in Anesthesia

NCT07661186 | Not Yet Recruiting

• 1 other identifier: st05
• Study Type: observational
• Target: 165
• Locations: 0 countries
• Sites: N/A

Brief Summary

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.

Conditions

Laparoscopic

Outcome Measures

Primary Outcomes (2)

• 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.

  1 day

• primaty

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

  1 day

Study Arms (3)

group laryngoscopy

usin laryngoscopy

group videolaryngoscopy

using videolaryngoscopy

group fiberoptic bronchoscopy

using fiberoptic bronchoscopy

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

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

You may qualify if:

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

You may not qualify if:

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

Sponsors & Collaborators

• Amasya University: lead

Related Publications (1)

• el-Ganzouri AR, McCarthy RJ, Tuman KJ, Tanck EN, Ivankovich AD. Preoperative airway assessment: predictive value of a multivariate risk index. Anesth Analg. 1996 Jun;82(6):1197-204. doi: 10.1097/00000539-199606000-00017.

  PMID: 8638791 BACKGROUND

Central Study Contacts

harun t duran, ass prof

CONTACT

905379856599; harun.duran@amasya.edu.tr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 1 Day
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 14, 2026
• First Posted: June 22, 2026
• Study Start: June 14, 2026
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): December 15, 2026
• Last Updated: June 22, 2026

Record last verified: 2026-06

Data Sharing

• IPD Sharing: Will not share