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The feasibility study of no indwelling or only intraoperative indwelling catheter in patients with pulmonary surgery during perioperative period

The feasibility study of no indwelling or only intraoperative indwelling catheter in patients with pulmonary surgery during perioperative period

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010816
Enrollment
Unknown
Registered
2017-03-08
Start date
2017-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Lung disease

Interventions

control group:Routine preoperative catheterization, catheter removal after 24-48 hours
Experimental group A:Routine preoperative catheterization and after anesthesia removal urethral catheter
Experimental group B:Perioperative no indwelling catheter

Sponsors

The First Affiliated Hospital of Medical School of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 70 Years

Inclusion criteria

Inclusion criteria: 1. patients who had no contraindication for pulmonary surgery and signed informed consent before operation; 2. The patients were operated under general anesthesia, 14F or 16F using Foley's catheter according to the situation after the success of anesthesia catheterization, ASA level i-ii; 3. VATS lobectomy, pulmonary resection or pulmonary wedge resection; 4. Less than 60 years old; 5. Operation time is less than 150 min; 6. All patients with preoperative exercise on the bed urination habits, all adapted to the bed of the urine habits.

Exclusion criteria

Exclusion criteria: 1. Patients with preoperative serious urinary tract disease (including urinary tract stones, infections and tumors, etc.)lead to difficult urination; 2. Suffering from heart, lung, kidney and other serious systemic disease; 3. The patient or his family refused to remove the catheter immediately after surgery; 4. Patients with obvious hyperplasia of prostate, chronic prostatitis and urinary retention; 5. History of lower urinary tract surgery; 6. Preoperative 48h catheterization history.

Design outcomes

Primary

MeasureTime frame
urinary tract infection rate;urinary retention;Comfortable degree;

Secondary

MeasureTime frame
length of stay;hospitalization expenses;Bed activity time;

Countries

China

Contacts

Public ContactJian Hu
hujian_med@163.com+86 13750801974

Outcome results

None listed

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