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UnknownNCT04440787

Prevention of Endotracheal Tube Migration by Cuff Palpation During Robotic Surgical Procedure

To Evaluate "Three Point Cuff Palpation Technique" for Assessing Optimal Depth of Endotracheal Tube Placement.

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Rajiv Gandhi Cancer Institute & Research Center, India · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

After intubation, the endotracheal tube was finally fixed after palpating endotracheal cuff at three sites (just below the cricoid cartilage, at suprasternal level and just below suprasternal notch). Fibre optic bronchoscopy will be done to find distance between tip of endotracheal tube and carina. This distance will be measured repeatedly, after pneumoperitoneum, after trendelenburg position and after making the patient supine at the end of surgery. Change in the distance will be noted.

Detailed description

The endotracheal tube (ETT) will be placed according to the black mark on the tube, post-intubation, the tube will be finally fixed after palpating endotracheal cuff at three sites (below cricoid cartilage, at suprasternal level and just below suprasternal notch). ETT cuff position will be scanned by sonography of airway to confirm the position of the proximal end of the ETT cuff. Fibre optic bronchoscopy will be done to find distance between tip of endotracheal tube and carina. This distance will be measured repeatedly 5 minutes after pneumoperitoneum, 10 minutes after trendelenburg position and 10 minutes after making the patient supine at the end of surgery. Change in the distance will be noted to confirm the migration of ETT.

Conditions

Interventions

TypeNameDescription
PROCEDUREThree point cuff palpation techniquethe ETT is finally positioned according to the Three point cuff technique.

Timeline

Start date
2018-12-01
Primary completion
2021-01-19
Completion
2021-03-31
First posted
2020-06-22
Last updated
2020-06-22

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT04440787. Inclusion in this directory is not an endorsement.