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Effect of Buccal Acupuncture on catheter-related bladder irritation after Ureteroscopic lithotripsy

Effect of Buccal Acupuncture on catheter-related bladder irritation after Ureteroscopic lithotripsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000302
Enrollment
Unknown
Registered
2024-08-26
Start date
2024-08-31
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

catheter-related bladder irritation

Interventions

experimental group,buccal acupuncture treatment group:Patients in the buccal acupuncture treatment group received buccal acupuncture therapy following extubation after surgery. The selected acupunctur
control group:Sham acupuncture: Upon completion of surgery and extubation in the control group patients, Gentian violet marker was used to mark the same acupoints as those in the buccal acupuncture tr

Sponsors

Department of Anesthesiology,the 924th Hospital of the PLA Joint Logistics Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Patients voluntarily participate and sign the informed consent form; 2) Age greater than 18 years; 3) Scheduled for elective ureteroscopic lithotripsy; 4) ASA I-III classification; 5) Requires indwelling catheter.

Exclusion criteria

Exclusion criteria: 1) Inability to communicate upon recovery in the post-anesthesia care unit (PACU), accompanied by cognitive dysfunction and emergence delirium in the PACU. 2) Presence of skin lesions or scarring at acupuncture points, or diagnosis of mumps. 3) Preoperative diagnosis of neurogenic bladder. 4) American Society of Anesthesiologists (ASA) Physical Status Classification of IV or higher, with severe hepatic or renal impairment. 5) Planned postoperative admission to the Intensive Care Unit (ICU) or unplanned transfer to the ICU. 6) Allergic reactions to standard general anesthetic agents, rendering the completion of surgical anesthesia impossible. 7) Concurrent participation in other clinical trials. 8) History of neurological or psychiatric disorders, or any other conditions that prevent compliance with follow-up.

Design outcomes

Primary

MeasureTime frame
Classification of Postoperative Catheter-Related Bladder Discomfort (CRBD);

Secondary

MeasureTime frame
Richmond Agitation and Sedation Scale,RASS;Assessment of Postoperative Sleep Quality;Assessment of Postoperative Recovery Quality;Assessment of Nausea, Vomiting, and Quality of Gastrointestinal Recovery;postoperative complications;first time of out-of-bed activity after surgery;postoperative satisfaction;Total hospitalization cost;first time of eating after surgery;Quality of Anesthetic Recovery;hospitalization time after surgery;Pain Intensity Score;The first time of flatus and bowel movement after surgery;consumption of postoperative analgesic;

Countries

China

Contacts

Public ContactWang Dong

The 924th Hospital of the PLA Joint Logistics Support Force

376553370@qq.com+86 181 7737 9009

Outcome results

None listed

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