NCT03373617

Completed

The Effect of Anesthesia Type on RIRS

Seoul National University Hospital Source

Other study identifiers

Sponsor study identifier

20-2017-10

Study Type

observational

Actual enrollment (reported)

66

Locations

1 country

Sites

1

Timeline

Study Start

December 13, 2017

Actual (reported)

Primary Completion

December 28, 2018

Actual (reported)

Study Completion

January 14, 2019

Actual (reported)

Brief Summary

Retrograde intrarenal surgery (RIRS) with flexible ureteroscopy is based on video monitoring of urinary tract during operation. Therefore, shaking vision on monitor can bother surgeons and make them tired. This can lead in tissue injury from lasing. The purpose of this study is to investigate the stability of monitoring of surgical field which is assessed by surgeon.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 66 participants
Study completion date: January 14, 2019
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
December 11, 2017
Actual (reported)
Study Start
December 13, 2017
Actual (reported)
First Posted
December 14, 2017
Actual (reported)
Primary Completion
December 28, 2018
Actual (reported)
Study Completion
January 14, 2019
Actual (reported)

Last Updated: July 23, 2021
Status Verified: July 2021
Last Update Submitted: July 22, 2021

Conditions

Renal Stone

Outcome Measures

Primary Outcomes (1)

VAS for stability of monitoring
VAS (from 1 to 10) for stability in monitoring of surgical field, which is assessed by surgeons
intraoperative

Study Arms (2)

General anesthesia group

Patients in general anesthesia group are scheduled to undergo RIRS under general anesthesia.

Spinal anesthesia group

Patients in spinal anesthesia group are scheduled to undergo RIRS under spinal anesthesia

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodProbability Sample

Study Population

Patients requiring RIRS because of renal stone

You may qualify if:

Patients requiring RIRS because of renal stone.

You may not qualify if:

Sponsors & Collaborators

Seoul National University Hospital
Otherlead
SMG-SNU Boramae Medical Center
Othercollaborator

Study Sites (1)

Seoul Metropolitan Government Seoul National University Boramae Medical Center

Seoul, 07061, South Korea

MeSH Terms

Conditions

Nephrolithiasis

Condition Hierarchy (Ancestors)

Kidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesUrolithiasisMale Urogenital Diseases

Study Officials

Jung-Man Lee, M.D.,PhD
SMG-SNU Boramae Medical Center
PRINCIPAL INVESTIGATOR

Enrollment

66 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Target Duration: 1 Week
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Clinical assistant professor

Study Record Dates

First Submitted

December 11, 2017

First Posted

December 14, 2017

Study Start

December 13, 2017

Actual (reported)

Not Applicable

Completed

NCT03046888

ROBOTIC PYELOLITHIOTOMY VERSUS PERCUTANEOUS NEPHROLITHOTOMY (PCNL).

Not ApplicableCompleted

NCT03189264

Percutaneous Nephrolithotomy for Treatment of Kidney Stones Greater Than 2 cm

Not ApplicableUnknown

NCT07411391

Supervised Endoscopic Tele-controlled Intelligent Lithotripsy

Not ApplicableRecruiting

NCT05384197

Enhanced Versus Extended Preoperative Antibiotic Prophylaxis Regimens for Retrograde Intrarenal Surgery in High Infectious Risk Patients

Phase 3Unknown

NCT03828175

Basic Hemodynamic Monitoring Reliability During Percutaneous Nephrolithotomy.

Not ApplicableCompleted

NCT06786715

Retrograde Intrarenal Surgery (RIRS) With Suction

Not ApplicableActive Not Recruiting

disagreement for the trial.

Contact the study team to confirm eligibility.

Primary Completion

December 28, 2018

Actual (reported)

Study Completion

January 14, 2019

Actual (reported)

Last Updated

July 23, 2021

Record last verified: 2021-07

Source record

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Source: ClinicalTrials.gov.

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Registry identifier: NCT03373617
Data provider: ClinicalTrials.gov
Source updated: 2021-07-23
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:21:34 UTC

Locations

KR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (2)

General anesthesia group

Spinal anesthesia group

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations