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Transcutaneous acupoint electrical stimulation for prevention of catheter-related bladder discomfort after ureteroscopic laser lithotripsy

A randomized, double blind, controlled trial for transcutaneous acupoint electrical stimulation as a prevention for catheter-related bladder discomfort duiring anesthesia recovery period in the patients who underwent ureteroscopic laser lithotripsy under general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020052
Enrollment
Unknown
Registered
2018-12-12
Start date
2018-12-12
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

catheter-related bladder discomfort

Interventions

TEAS group:Transcutaneous acupoint electrical stimulation
Control group:Connect the instrument but do not give electrical stimulation

Sponsors

General Hospital of Northern Theater Command of the Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. patients who will undergo selective ureteroscopic laser lithotripsy under general anesthesia; 2. Aged 18-70years old males; 3. BMI:18-30kg/m2,ASA:I-III; 4. Fully understand about the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Mental system diseases (such as schizophrenia, depression, etc.) and cognitive dysfunction; 2. Severe cardiovascular and cerebrovascular diseases (such as myocardial infarction, unstable angina, stroke with severe sequelae); 3. Have participated in other drug or device clinical trials within 3 months before surgery; 4. Infection or previous surgical scar at the needle site; 5. The researchers think that patients are not suitable for transcutaneous acupoint electrical stimulation.

Design outcomes

Primary

MeasureTime frame
catheter-related bladder discomfort;—

Secondary

MeasureTime frame
Anesthetic dose;Time of wake up;PONV;Postoperative skin itching;POCD;Postoperative sedation score;Postoperative pain score (VAS);—

Countries

China

Contacts

Public ContactLi Lin

General Hospital of Northern Theater Command of the Chinese People's Liberation Army

lin.1975@hotmail.com+86 13304042711

Outcome results

None listed

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