Skip to content

Clinical study on the relationship between continuous balloon pressure control and postoperative laryngeal pain

Clinical study on the relationship between continuous balloon pressure control and postoperative laryngeal pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107174
Enrollment
Unknown
Registered
2025-08-05
Start date
2025-08-30
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Postoperative sore throat

Interventions

Group P:Connect the continuous pneumatic bladder pressure control device, continuously monitor and automatically adjust the pressure (target 25 cmH2O, allowing +/-2 cmH2O fluctuation).
Group C:Inject 2-3 ml of air into the balloon manually using the traditional method.

Sponsors

Guangzhou Women and Children's Medical Center, Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. scheduled for general anesthesia with tracheal intubation surgery (expected intubation time >= 3 hours); 3. American Society of Anesthesiologists (ASA) classification I-II.

Exclusion criteria

Exclusion criteria: 1. Preoperative presence of throat diseases or recent intubation history (within 14 days); 2. Abnormal tracheal anatomy (such as stenosis, tumors); 3. Emergency surgery; 4. Anticipated need for long-term mechanical ventilation after surgery.

Design outcomes

Primary

MeasureTime frame
Postoperative laryngeal pain;

Secondary

MeasureTime frame
Severity of sore throat;Airbag pressure fluctuation range;The incidence of hoarseness or cough after surgery;Adverse events (such as airbag leakage, tracheal mucosal injury);

Countries

China

Contacts

Public ContactQianqi Qiu

Guangzhou Women and Children's Medical Center, Guangzhou Medical University

qiuqianqi1216@sina.com+86 136 3239 1377

Outcome results

None listed

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