LaparoscopicNCT07661186
Clinical Outcomes of Intubation Techniques in Anesthesia
An observational study of Laparoscopic, run by Amasya University.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Laparoscopic
- How many people
- 165 participants
- Where
- No sites listed yet
- Study dates
- 14 Jun 2026to 15 Dec 2026
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: This study aims to determine the incidence of postoperative cough and sore throat using endotracheal intubation techniques in laparoscopic cholecystectomy surgeries.
Who may be able to join
- Patients over 18 years of age ASA 1-2-3 patients undergoing elective laparoscopic cholecystectomy surgery Patients who agreed to participate in the study
Who cannot join
- Patients for whom difficult intubation is considered Patients with neurological disorders Patients with mental retardation Patients who refused to participate in the study.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Clinical Outcomes of Intubation Techniques in Anesthesia; an Observational Study.
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.
Read the detailed description
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.
- Conditions
- Laparoscopic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| group laryngoscopy | usin laryngoscopy | |
| group videolaryngoscopy | using videolaryngoscopy | |
| group fiberoptic bronchoscopy | using fiberoptic bronchoscopy |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: 1 day
primaty
The primary objective of the study is to evaluate the intubation success rates of three different intubation techniques.
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jun 2026
- Study start14 Jun 2026 (estimated)
- Primary completion1 Dec 2026 (estimated)
- Study completion15 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for LaparoscopicStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 165 participants (estimated)
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Amasya University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07661186
- Sponsor's protocol ID
- st05
- Status last verified
- Jun 2026
- First submitted
- 14 Jun 2026
- Last updated
- 22 Jun 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
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.
PubMed 8638791
Study at a glance
From the registry record, last updated by the sponsor on 22 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Outcomes of Intubation Techniques in Anesthesia; an Observational Study.
- ClinicalTrials.gov ID
- NCT07661186
- Acronym / sponsor ID
- st05
- Conditions
- Laparoscopic
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 165 participants (estimated)
- Lead sponsor
- Amasya UniversityUniversity, hospital or other
- Study start
- 14 Jun 2026 (estimated)
- Primary completion
- 1 Dec 2026 (estimated)
- Study completion
- 15 Dec 2026 (estimated)
- First posted
- 22 Jun 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Day
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| group laryngoscopy | – | –usin laryngoscopy |
| group videolaryngoscopy | – | –using videolaryngoscopy |
| group fiberoptic bronchoscopy | – | –using fiberoptic bronchoscopy |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- This study aims to determine the incidence of postoperative cough and sore throat using endotracheal intubation techniques in laparoscopic cholecystectomy surgeries.
Key inclusion criteria (1 listed)
- Patients over 18 years of age ASA 1-2-3 patients undergoing elective laparoscopic cholecystectomy surgery Patients who agreed to participate in the study
Key exclusion criteria (1 listed)
- Patients for whom difficult intubation is considered Patients with neurological disorders Patients with mental retardation Patients who refused to participate in the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
sore throat
Time frame: 1 day
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.
primaty
Time frame: 1 day
The primary objective of the study is to evaluate the intubation success rates of three different intubation techniques.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jun 2026.
- Background: PubMed 8638791el-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.
- Individual participant dataSharing planned: No
Related trials for Laparoscopic
Active, not recruiting
Efficacy of Laparoscopic-Assisted TAP Block in Laparoscopic Appendectomy
Appendectomy, Laparoscopic, Blockades Neuromuscular
Recruiting
Study of the Influence of Intraperitoneal Insufflation of CO2 by Laparoscopy on the Short-term Evolution of Premature Infants With Ulcerative Necrotizing Enterocolitis
Preterm Birth, Enterocolitis, Necrotizing
RecruitingObservational study
Two-Year Weight Loss With GLP-1 Medications Compared With Sleeve Gastrectomy in Adults With Obesity
Obesity & Overweight
Recruiting
Efficacy of Ovarian Drilling Via vNOTES Laparoscopy in Patients With PCOS
PCOS (Polycystic Ovary Syndrome)
Not yet recruitingPhase 4
Effect of Prophylactic Dexamethasone vs Placebo on Airway Dimensions Assessed by Ultrasonography in Patients Undergoing Laparoscopic Cholecystectomy
Airway Edema, Postoperative Complications
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
An observational study of Laparoscopic, run by Amasya University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 22 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact harun t duran, ass prof (905379856599, harun.duran@amasya.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
sore throat (time frame: 1 day). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07661186, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2026.