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Effects of Silicone Double Cavity Tracheal Catheter and PVC Double Cavity Tracheal Catheter on the Incidence of Throat Pain After Thoracoscopic Pulmonary Surgery

Effects of Silicone Double Cavity Tracheal Catheter and PVC Double Cavity Tracheal Catheter on the Incidence of Throat Pain After Thoracoscopic Pulmonary Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093117
Enrollment
Unknown
Registered
2024-11-28
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Pulmonary disease

Interventions

Experimental Group:Choosing a Silicone Double Cavity Tracheal Catheter
Control group:Selecting a PVC Double Cavity Tracheal Catheter

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Intended thoracoscopic assisted lung surgery; 2.Age 18-80; 3.ASA Level I-III; 4.Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Anticipate difficult airway; 2.Chronic laryngitis, chronic bronchitis, asthma, gastroesophageal reflux; 3.Upper respiratory tract infection within 1 month before surgery; 4.Previous thoracoscopic assisted lung surgery.

Design outcomes

Primary

MeasureTime frame
The incidence of sore throat within 24 hours and 48 hours after surgery;—

Secondary

MeasureTime frame
Postoperative hoarseness;Postoperative nausea and vomiting;—

Countries

China

Contacts

Public ContactXu Pingbo

Zhejiang Cancer Hospital

xupingboshanghai@163.com+86 18017312996

Outcome results

None listed

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