Oral Fluid Intake After Extubation

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-02-01

Study Completion Date

2024-10-16

Brief Summary

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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their side effects changed significantly from their first usage, the investigators can assume that existing approach is obsolete and has no place anymore in the modern medicine.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.

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Detailed Description

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Everything stated in the brief summary.

Conditions

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Intubation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Early fluid intake

Group Type EXPERIMENTAL

Fluid intake not as per standard guidlines

Intervention Type BEHAVIORAL

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.

Standard Delayed oral fluid

Group Type OTHER

Fluid intake not as per standard guidlines

Intervention Type BEHAVIORAL

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.

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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

Eligible Sex

ALL

Accepts Healthy Volunteers

No