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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03957109
Other study ID # 16-2015-75
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 18, 2015
Est. completion date February 10, 2017

Study information

Verified date May 2019
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients who underwent retrograde intrarenal surgery (RIRS) were randomly allocated to general anesthesia (GA) or spinal anesthesia (SA) groups. Renal function was assessed using estimated glomerular filtration rate, and relative renal function was evaluated using nuclear medicine tests. Maneuverability and accessibility were evaluated after every surgery. We analyzed the influence of anesthesia methods on surgical outcomes and renal function in retrograde intrarenal surgery in a prospective, randomized controlled study.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date February 10, 2017
Est. primary completion date February 10, 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - older than 20 years with renal stones greater than 10 mm Exclusion Criteria: - patients who have urologic anatomical abnormalities - patients with ASA status = grade III, a contraindication for spinal anesthesia or RIRS, or unexpected intraoperative renal injury

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
general anesthesia


Locations

Country Name City State
Korea, Republic of Seoul National University 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 Renal function change according to anesthesia method using nuclear medicine tests with diethylenetriamine pentaacetic acid (99m Tc-DTPA) prior to procedure, and at 3 months after the procedure.
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