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Enrolling by Invitation

NCT Number: NCT07157917

Thirst Translation and RCT

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

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Taiwan University

Taipei, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Protocol based

Other

Apply a thirst safety management protocol

Control

Other

Room air water

Primary outcomes

  1. Thirst intensity visual analogue scales

    Time frame: 0, 15, 60 minutes

    This is a 0~10 point Likert scale, with 0 indicates no thirsty, and 10 indicates the most severe thirsty.

Sponsors and collaborators

Lead sponsor

National Taiwan University

Other

Collaborators

  • National Taiwan University Hospital

Registry information

Official study title

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

Acronym: SEDE

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Sep 5, 2025
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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