Oral Fluid Intake After Extubation

Intubation Clinical Trial

Official title:

Early Versus Delayed Oral Fluid Intake Initiation (Sipping) After Extubation, Influence on the Feeling of Thirst, Patient Comfort and the Occurrence of Complications.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05819645
• Other study ID #: EK-1381/22
• Status: Recruiting
• Phase: N/A
• Start date: February 1, 2023
• Est. completion date: February 1, 2025

Study information

• Verified date: April 2023
• Source: University Hospital, Motol
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

According to the current guidelines the patient is not allowed to drink any fluid at least 2 hours after extubation to prevent complications. However there is no evidence in the literature to support this approach. Because anaesthetic drugs and their side effects changed significantly from their first usage, the investigators can assume that existing approach is obsolete and has no place anymore in the modern medicine. Keeping patient n.p.o (nothing per os) for 2 hours after extubation may lead to patient´s thirst or other discomfort. The aim of the study is to detect whether early oral fluid intake after extubation could lead to safe relief of thirst and to better patient´s comfort overall.

Description:

Everything stated in the brief summary.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 160
• Est. completion date: February 1, 2025
• Est. primary completion date: January 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• patients with planned extubation assigned to the study
• able to swallow the fluid
• willing to participate the study

Exclusion Criteria:

• patients after upper digestive tract surgery
• patients after trachea surgery
• patients with possible neurological deficiency
• patients after VIII. cranial nerve surgery
• patients not able to swallow

Related Conditions & MeSH terms

• Intubation

Intervention

Behavioral:
• Fluid intake not as per standard guidlines
The participant will be randomized into two arms. After the randomization one arm will get the per os fluid intake before the standard time frame.

Locations

Country	Name	City	State
Czechia	University Hospital Motol, Charles University in Prague	Prague	Czech Republic

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Motol

Country where clinical trial is conducted

Czechia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of presence or absence of thirst 120 minutes after extubation	Between both groups the presence of anpleasent feeling of thirst will be assessed and compared	During procedure (120 minutes after extubation)