Clinical Study on Targeted Bladder Thermotherapy for Prevention of Emergence Agitation in Patients Undergoing Indwelling Urinary Catheterization Under General Anesthesia

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500103315

Enrollment

Unknown

Registered

2025-05-27

Start date

2025-05-31

Completion date

Unknown

Last updated

2025-06-02

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

Conditions

Emergence Agitation

Interventions

Hot Compress Group:Use an intelligent temperature-control device to perform hot compress on the bladder area of enrolled patients.

Control group:No hot compress measures are applied.

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-75 years, undergoing elective surgery under general anesthesia with an indwelling urinary catheter; (2) ASA physical status classification grades I-III; (3) Having signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Complicated with severe cardiopulmonary or renal insufficiency; (2) History of bladder surgery or organic lesions in the bladder or urethra; (3) Local skin damage or thermosensitive constitution; (4) Preoperative use of anticholinergic drugs or a-blockers; (5) Suffering from neuropsychiatric diseases or cognitive dysfunction, unable to accurately express their own feelings; (6) Patients undergoing urological or gynecological surgery.

Design outcomes

Primary

Measure	Time frame
Catheter-Related Bladder Discomfort ;Incidence of emergence agitation;	—

Secondary

Measure	Time frame
Catheter-related complications (infection, urethral injury, etc.);Comfort;Satisfaction;	—

Countries

China

Contacts

Public ContactXu Zhipeng

Affiliated Hospital of Jiangsu University

xu630371236@163.com+86 152 6292 1001

Outcome results

None listed

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