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Study for nursing effect of secondary dry mouth disease in critical patients in ICU

Study for nursing effect of secondary dry mouth disease in critical patients in ICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022873
Enrollment
Unknown
Registered
2019-04-28
Start date
2017-06-01
Completion date
Unknown
Last updated
2019-05-05

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

Conditions

critical illness

Interventions

experimental group:Peppermint water, vitamin C spray and lip balm
Control group:Oral care using warm water

Sponsors

Ruijin hospital affiliated to Shanghai jiaotong university school of medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Fasting patients of ICU; 2. The ICU treatment time longer than 24 hours; 3. Aged 18 years and more; 4. Clear consciousness and good coordination; 5. Sign the informed consent form and voluntarily participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with persistent and refractory dry mouth, including: (1) head and neck tumor treatment; (2) systemic diseases; (3) The hemodialysis patient; (4) special drugs: anti-anxiety drugs, antidepressants and psychotropic drugs, antihypertensive drugs, receptor and receptor blockers; 2. Patients who are unable to communicate verbally include patients with mechanical ventilation, consciousness disorder, cognitive disorder and mental illness.

Design outcomes

Primary

MeasureTime frame
visual analogue scale;condition of lips, tongue and oral mucosa moisture;condition of lips, tongue and oral mucosa moisture;

Countries

China

Contacts

Public ContactYanting Gu

Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine

gyt21802@rjh.com.cn+86 15821016224

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026