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Effects of a spray-based oropharyngeal training programme for patients after cardiac surgery following endotracheal extubation in the intensive care unit

Risk factors for thirst in the intensive care unit and application of thirst intervention for ICU patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16009108
Enrollment
Unknown
Registered
2016-08-28
Start date
2016-10-31
Completion date
Unknown
Last updated
2021-07-21

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

Conditions

critical diseases

Interventions

SOTP-A group:a three-part programme offering spray-based therapy, provided as a constant low-temperature cold spray (programme A)
SOTP-B group: three-part programme offering spray-based therapy, provided as a low-to-normal temperature spray (programme B)
control group:usual care-provided wet cotton swabs to moisten their mouths

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 01 Observational studyt: The inclusion criteria for patient were as follows: 1) age >= 18 years; 2) length of ICU stay >= 24 h; 3) conscious during the assessment (Richmond Agitation–Sedation Scale [RASS] score -1 to +1); 4) able to communicate verbally and understand the questionnaires; and 5) agreed to participate in the study. 02 Intervention Study: All ICU patients who underwent cardiac surgery and received MV at the cardiovascular surgery department.

Exclusion criteria

Exclusion criteria: 01 Observational study: The exclusion criteria were as follows: 1) unable to complete the assessment; and 2) transferred out of the ICU during the study. 02 Intervention Study: Patients accept intervention were excluded if they: (1) had a history of neuromuscular disease (e.g. stroke, Parkinsonism) or head and neck deformities; (2) had a pre-existing swallowing difficulty; (3) received tracheostomy; (4) could not respond to questions/intervention; and (5) were absolutely quarantined (e.g. for open or infectious tuberculosis).

Design outcomes

Primary

MeasureTime frame
0–10 numeric rating scale (NRS);Perioperative Thirst Discomfort Scale (PTDS);

Secondary

MeasureTime frame
incidence of dysphagia;adverse events;

Countries

China

Contacts

Public ContactLi Hong

Fujian Provincial Hospital

leehong99@126.com+86 13705070219

Outcome results

None listed

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