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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02252445
Other study ID # CRBDPPFSEVO
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 26, 2014
Last updated September 29, 2014
Start date October 2014
Est. completion date March 2015

Study information

Verified date September 2014
Source Seoul National University Hospital
Contact Hyun-Chang Kim, MD
Phone 82-10-2886-2876
Email onidori1979@gmail.com
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The investigators want to evaluate the efficacy of the propofol and sevoflurane for the prevention of catheter-related bladder discomfort.


Description:

The mechanism of catheter-related bladder discomfort is thought to be related to the muscarinic receptor. Propofol and desflurane are most widely used as an anesthetic agent. Propofol and desflurane are known to block the muscarinic receptor in different ways.

The investigators want to evaluate the efficacy of the propofol and sevoflurane for the prevention of catheter-related bladder discomfort.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 76
Est. completion date March 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients scheduled for transurethral bladder excision under general anesthesia

- ASA I-III

Exclusion Criteria:

- Foley catheter less than 18 Fr.

- Patients with obstruction of urinary tract

- Patients with neurogenic bladder

- Patients with severe obesity

- Patients with neurologic disorder

- Patients with chronic pain

- Patients with allergic history to propofol or sevoflurane

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Intervention

Drug:
Propofol
Propofol will be administered.
Sevoflurane
Sevoflurane will be administered.

Locations

Country Name City State
Korea, Republic of Seolu National University of Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Catheter-related bladder discomfort Catheter-related bladder discomfort will be measured at 1 hour postoperatively (0:none, 1:mild, 2:moderate, 3:severe). 1 hour postoperatively No
Secondary Catheter-related bladder discomfort Catheter-related bladder discomfort will be measured at 1 hour postoperatively (0:none, 1:mild, 2:moderate, 3:severe). 0, 6 and 24 hour postoperatively No
Secondary Hemodynamic parameters Mean blood pressure and heart rate will be measured at 0, 1, 5, 10 minute postoperatively. Measurement at 10 minute means Mean blood pressure and heart rate at the admission of post-anesthetic care unit. 0, 1, 5, 10 minute postoperatively No
Secondary Nausea Nausea will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
Secondary Vomiting Vomiting will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
Secondary Dry mouth Dry mouth will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
Secondary Flushing Flushing will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
Secondary Blurred vision Blurred vision will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
Secondary Dizziness Dizziness will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
Secondary Analgesics The amount of analgesics will be measured at 0, 1, 6 and 24 hour postoperatively. 0, 1, 6 and 24 hour postoperatively No
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