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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06405672
Other study ID # 1/17
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 30, 2024
Est. completion date September 30, 2024

Study information

Verified date April 2024
Source Antalya Training and Research Hospital
Contact Kerem Inanoglu, MD
Phone +902422494400
Email kinanoglu@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators aimed to compare the effects of using enotracheal tube with stylet versus endotracheal tube alone in morbidly obese patients undergoing sleeve gastrectomy.


Description:

Different intubation techniques have been used in morbidly obese patients undergoing general anesthesia. No study comparing the use of endotracheal tube with or without stylet was found in literature. Thus, the investigators aimed to compare the effects of using enotracheal tube with stylet versus endotracheal tube alone in morbidly obese patients undergoing sleeve gastrectomy.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 80
Est. completion date September 30, 2024
Est. primary completion date August 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: Body mass index over 30 ASA physical status I-III Undergoing laparoscopic sleeve gastrectomy - Exclusion Criteria: Body mass index under 30 ASA physical status IV Unable to cooperate Refused to give writtten informed consent-

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Endotracheal tube with stylet
The obese patients who will be intubated with stylet in laparoscopic sleeve gastrectomy
Endotracheal tube alone
The obese patients who will be intubated without stylet in laparoscopic sleeve gastrectomy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Antalya Training and Research Hospital

References & Publications (2)

Gaszynski T, Pietrzyk M, Szewczyk T, Gaszynska E. A comparison of performance of endotracheal intubation using the Levitan FPS optical stylet or Lary-Flex videolaryngoscope in morbidly obese patients. ScientificWorldJournal. 2014;2014:207591. doi: 10.1155/2014/207591. Epub 2014 May 20. — View Citation

Nicholson A, Smith AF, Lewis SR, Cook TM. Tracheal intubation with a flexible intubation scope versus other intubation techniques for obese patients requiring general anaesthesia. Cochrane Database Syst Rev. 2014 Jan 17;(1):CD010320. doi: 10.1002/14651858.CD010320.pub2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Intubation time from handling laryngoscope to first vision of end-tidal CO2 waveform through study completion, an average of 6 months
Secondary Intubation success success or failure of first intubation attempt through study completion, an average of 6 months
Secondary complications Undesirable complications such as laryngospazm, hoarseness will be recorded at postoperative period through study completion, an average of 6 months
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