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A clinical study of different doses of butorphanol combined with dexmedetomidine for the treatment of catheter-related bladder irritation

A clinical study of different doses of butorphanol combined with dexmedetomidine for the treatment of catheter-related bladder irritation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091174
Enrollment
Unknown
Registered
2024-10-22
Start date
2024-10-25
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

catheter-related bladder irritation(CRBD)

Interventions

D Group:Intravenous injection of dexmedetomidine 0.2µg/kg at 1 minute
DLB Group:Intravenous injection of dexmedetomidine 0.2µg/kg and butorphanol tartrate 10ug/kg at 1 minute
DHB Group:Intravenous injection of dexmedetomidine 0.2µg/kg and butorphanol tartrate 20ug/kg at 1 minute

Sponsors

Department of Anesthesiology, Yijishan Hospital, Wannan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-70 years old, male or female (2) ASA Grade I-III (3) Patients with catheterization after general anesthesia induction (4) Sign informed consent

Exclusion criteria

Exclusion criteria: (1) Patients with bladder outflow tract obstruction, urinary tract infection, neurogenic bladder and prostatic hyperplasia (2) Patients taking anti-inflammatory drugs, opioid analgesics, sedatives, antidepressants, immunomodulators and other drugs for a long time (3) Patients with a history of cerebrovascular disease, cardiovascular disease, and mental illness (4) Patients with severe liver and kidney diseases and severe conduction block (5) Patients with severe impairment of hearing or communication or cognitive function (6) Patients who are also participating in other trial studies

Design outcomes

Primary

MeasureTime frame
Remission of CRBD within 30 minutes of administration in all three groups;

Secondary

MeasureTime frame
CRBD remission at 1 hour, 6 hours, and 24 hours of administration in three groups;NRS scores were obtained for 0 minutes, 5 minutes, 15 minutes, 30 minutes, 1 hour, 6 hours, and 24 hours;Three groups of patients were given 0 minutes, 5 minutes, 15 minutes, 30 minutes, 1 hour, 6 hours, 24 hours of SAS scores;Mean arterial pressure, heart rate, and pulse oxygen saturation were measured at 0 minutes, 5 minutes, 15 minutes, 30 minutes, 1 hour, 6 hours, and 24 hours;The incidence of respiratory depression (SpO2<90%), nausea and vomiting, dry mouth, chills and delirium, dizziness and headache after administration in the three groups;15 Quality of recovery scores (QoR-15) 24 hours after surgery in all three groups;

Countries

China

Contacts

Public ContactWang Yulong

Department of Anesthesiology,Yijishan Hospital, Wannan Medical College

dr_wangyulong@163.com+86 180 5531 7805

Outcome results

None listed

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