Menu
Not yet recruiting NCT07690475

Development and Application of an Oral Care Protocol for Stroke Patients With Orotracheal Intubation

No phase Interventional Develop an Oral Care Plan and Verify it

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: Standardized oral care protocol, Regular oral care.
Who it may be relevant to
Registry conditions: Develop an Oral Care Plan and Verify it. Basic parameters: from 18 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
Center list to be confirmed — check the primary protocol.
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 →

Overview

Develop a standardized oral care protocol for stroke patients undergoing orotracheal intubation based on evidence-based practice, and validate its effectiveness through clinical trials.

Interventions

  • Other Standardized oral care protocol
    Carry out oral care using the constructed standardized oral care plan
  • Other Regular oral care
    Carry out oral care using conventional methods

Primary outcome measures

  • Incidence of Ventilator-Associated Pneumonia (VAP) [Time frame: From intubation until extubation or discharge from ICU, up to 28 days.]

Eligibility criteria

Inclusion criteria

  • Diagnosed as a patient with stroke;Maintaining an oral tracheal tube insertion;The indwelling time of the oral tracheal tube should be at least 7 consecutive days;No oral diseases before intubation;Tooth count ≥ 10

Exclusion Criteria:The patient had been intubated for more than 48 hours before admission;Patients who have had their endotracheal tubes replaced during the procedure;Patients who were discharged halfway through their treatment

\-

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
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07690475 · KY-2026-099

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗