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The effect of early ice on oropharyngeal comfort and recovery of laryngeal function in patients after extubation

Construction and application of extubation protocol for adult tracheal intubation patients in ICU

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060008
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-10
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Experimental group:Give a small amount of ice in the mouth as soon as possible after routine oral care in patients with tracheal extubation
Control group:Continue fasting for 6 hours after routine oral care (routine care)

Sponsors

Gansu Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 65 years; 2. No pharyngeal disease or pain before endotracheal intubation; 3. Patients with an awareness or sedation score (RASS) of -2 to 1, who were cooperative, voluntarily entered the study and signed informed consent were eligible.

Exclusion criteria

Exclusion criteria: 1. Preexisting cognitive impairment or communication/language impairment; 2. Use of nasal tracheal tubes during ICU stay (i.e., only oral tracheal tubes are included); 3. Current or previous tracheotomy; 4. Inability to eat or drink by mouth due to medical conditions or surgery; 5. Can't stand ice; 6. Unstable and life-threatening vital signs after extubation; 7. Pre-existing or co-existing conditions that affect swallowing, such as head and neck surgery or trauma, oropharyngeal or esophageal tumors, and neuromuscular diseases.

Design outcomes

Primary

MeasureTime frame
Intensity of thirst;Perioperative thirst discomfort;Oropharyngeal comfort;Sore throat;

Secondary

MeasureTime frame
Hoarseness;Difficulty swallowing;

Countries

China

Contacts

Public ContactFan Luo
2569869312@qq.com+86 13909316149

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026