Skip to content

Perioperative of elderly patients undergoing painless endobronchial ultrasound-guided transbronchial needle aspiration construction and empirical study of enhanced recovery nursing program

Perioperative of elderly patients undergoing painless endobronchial ultrasound-guided transbronchial needle aspiration construction and empirical study of enhanced recovery nursing program

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091965
Enrollment
Unknown
Registered
2024-11-06
Start date
2024-04-30
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Endobronchial ultrasound-guided transbronchial needle aspiration

Interventions

Control group:The control group was treated with conventional painless ultrasonic bronchoscopy nursing.
Intervention group:The intervention group was treated with painless ultrasonic bronchoscopy for enhanced recovery nursing.

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) It meets the indications for painless ultrasonic bronchoscopy under general anesthesia, and needle-aspiration biopsy is required; (2) Clear mind, normal hearing and language expression ability; (3) Age =60 years old; (4) Planned operation time >30min.

Exclusion criteria

Exclusion criteria: (1) Patients allergic to anesthetic drugs treated with painless bronchoscopy; (2) Patients with other serious cardiovascular and cerebrovascular diseases, serious damage to liver and kidney function or obvious bleeding tendency and other blood system diseases, poor general conditions and other serious diseases; (3) Patients with complex bronchoscopy requiring multidisciplinary joint treatment.

Design outcomes

Primary

MeasureTime frame
Effects of different protocols on postoperative cough of patients: The scores of cough symptoms at 2h (T2), 6h(T6) and 24h(T24) after surgery and the incidence of cough within 24h after surgery in both groups.;

Secondary

MeasureTime frame
Effects of different programs on postoperative sore throat;Effects of different regimens on postoperative gastrointestinal reactions;Effect of different regimens on postoperative fever reaction;Evaluation of postoperative recovery quality by different regimens;Effects of different regimens on patient satisfaction scores;

Countries

China

Contacts

Public ContactChen Bi

Affiliated Hospital of Xuzhou Medical University

Chenbi207@126.com+86 150 0520 7551

Outcome results

None listed

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