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Catheter related bladder discomfort and transcutaneous electrical stimulatio

Not Applicable
Completed
Conditions
Neoplasms
Registration Number
KCT0007450
Lead Sponsor
Asan Medical Center
Brief Summary

TENS reduced moderate to severe CRBD, decreased postoperative pain, and increased patient satisfaction after TURBT.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
112
Inclusion Criteria

1) Transurethral resection of bladder tumor under general anesthesia
2) 20 years = age < 80 years
3) American society of anesthesia (ASA) classification 1 - 3
4) Patients who voluntarily agreed to this clinical study

Exclusion Criteria

1) Change to surgical plan to open surgery
2) Overactive bladder, neurogenic bladder, baldder outflow obstruction
3) Skin lesion on the buttock area
4) Pregnancy
5) History of seizure
6) Pacemaker insertion state
7) Refusal of patient

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of catheter related bladder discomfort above moderate grade
Secondary Outcome Measures
NameTimeMethod
Incidence of catheter related bladder discomfort above moderate grade;Incidence of catheter related bladder discomfort above moderate grade;Incidence of catheter related bladder discomfort above moderate grade;Numeric rating scale (NRS);Numeric rating scale (NRS);Global perceived effect scale (GPES);Analgesic dose during posoperative 24 hrs;Posoperative complications
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