Status:

UNKNOWN

Efficacy of Reduction of the Balloon Volume for Prevention of Postoperative Catheter-related Bladder Discomfort in Patients Undergoing Non-lower Urinary Tract Surgery

Lead Sponsor:

Buddhist Tzu Chi General Hospital

Conditions:

Catheter-Related Bladder Discomfort

Urinary Catheter

Eligibility:

All Genders

20-80 years

Phase:

NA

Brief Summary

CRBD is related to different degrees of irritation caused by the volume of the balloon in the urinary catheter, and when CRBD occurs, it may cause severe postoperative pain and trauma by self-removal ...

Detailed Description

Catheter-Related Bladder Discomfort (CRBD) has been attached importance in recent years. Reducing the discomfort of patients with effective treatment is a part of our medical and nursing care that nee...

Eligibility Criteria

Inclusion

  • age from 20-80 year-old
  • in urological surgery under the general anesthesia
  • 2 arms: (1)non-lower urinary tract surgery: hernia, and nephrectomy surgery , (2) lower urinary tract surgery: stone surgery after ureter catheter insertion.

Exclusion

  • Patients not undergoing hernia repair or nephrectomy.
  • Patients who are not undergoing ureteral lithotripsy and renal stone extraction.
  • Those who are already using drugs for overactive bladder or prostatic hypertrophy.
  • Retrograde intrarenal surgery (RIRS) for stone extraction.
  • People with dementia.
  • Patients with cognitive impairment.
  • Patients with impaired consciousness.
  • Patients who are unable to communicate verbally.
  • The subject had participated in other experimental drug trials one month before the study entered.

Key Trial Info

Start Date :

September 18 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2023

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT06038448

Start Date

September 18 2023

End Date

December 31 2023

Last Update

September 21 2023

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