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The effect of oral moisturizing spray on extubation outcomes

Investigating the Effect of Using Mouth Moisturizing Spray on the Outcomes of Cardiac Surgery Patients following Endotracheal Extubation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240408061453N1
Enrollment
40
Registered
2024-05-26
Start date
2024-05-21
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Nausea and vomiting. Nausea and vomiting

Interventions

Intervention 1: Control group: After the tube is removed, oral intake will begin 6 hours after the tube is removed. Critical care nurses will provide routine care, including moisturizing the mouth of

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Over 18 years old being literate in reading and writing Aware of time, place, and person Extubation of the patient after consciousness A patient undergoing coronary artery bypass surgery or valve replacement on pump.

Exclusion criteria

Exclusion criteria: History of neuromuscular disease (such as stroke, parkinsonism) or head and neck abnormalities. Have a swallowing problem before. Tracheostomy. Inability to respond verbally.

Design outcomes

Primary

MeasureTime frame
Thirst. Timepoint: Thirst evaluation will be done before the intervention, immediately after the first intervention, 2 and 4 hours after the intervention. Method of measurement: 10-point numerical rating scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAkbar Zare-Kaseb

Shahid Beheshti University of Medical Sciences

akbar.zarekaseb@gmail.com+98 938 699 0935

Outcome results

None listed

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