FindTrial
Sign In

Study on the Efficacy and Safety of Ultra-Early Cold Mint Spray for Postoperative Thirst in Patients Undergoing General Anesthesia

Study on the Efficacy and Safety of Ultra-Early Cold Mint Spray for Postoperative Thirst in Patients Undergoing General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116378
Enrollment
Unknown
Registered
2026-01-08
Start date
2026-01-10
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Surgical patients undergoing general anesthesia

Interventions

control group:Wet cotton swab moist lips
Cold mint spray group:The patient was extubated into the PACU and started after evaluation ( conscious, cough / swallowing according to instructions, no nausea and vomiting ). Intervention was perform
Cold purified water spray group:The patient was extubated into the PACU and started after evaluation ( conscious, cough / swallowing according to instructions, no nausea and vomiting ). Intervention w

Sponsors

Xuanwu Hospital of Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : 18-65 years old ; after general anesthesia into PACU ; aSA grade I-III.

Exclusion criteria

Exclusion criteria: Exclusion criteria : gastrointestinal surgery ; oral mucosal damage ; preoperative dysphagia ; communication barriers ; emergency surgery.

Design outcomes

Primary

MeasureTime frame
Thirst intensity;Thirst discomfort;Postoperative comfort;—

Countries

China

Contacts

Public Contactwangran

Xuanwu Hospital of Capital Medical University

wangran19831204@163.com+86 135 8182 7666

Outcome results

None listed

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