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Enrolling by invitation NCT07157917

Thirst Translation and RCT

No phase Interventional Thirst in Intensive Care Unit (ICU) Practice

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Protocol based, Control.
Who it may be relevant to
Registry conditions: Thirst in Intensive Care Unit (ICU) Practice. Basic parameters: 18 years — 100 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Translation and Application of the Chinese Thirst Safety Management Protocol: A Randomized Controlled Trial With Cultural Equivalence Validation Between Taiwan and Brazil

Overview

To translate the SEDE-E (Extubated) and SEDE-T(tracheotomized) protocols-Chinese version and validate it with an RCT trial

Interventions

  • Other Protocol based
    Apply a thirst safety management protocol
  • Other Control
    Room air water

Primary outcome measures

  • Thirst intensity visual analogue scales [Time frame: 0, 15, 60 minutes]

Eligibility criteria

Inclusion criteria

  • Patients whose physicians have issued orders for removal of the endotracheal tube or who have undergone tracheotomy,
  • patients with clear consciousness
  • patients who can communicate in Chinese as their native language

Exclusion criteria

  • patients with water restriction
  • patients who have undergone thirst quenching intervention measurements in the recovery room.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Taiwan · 1 center
  • National Taiwan University — Taipei

Identifiers

NCT: NCT07157917 · 202508163RIN

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗