Lithiasis, Urinary Clinical Trial
— EASILYOfficial title:
Evaluation of the Performance of a Robotic Flexible Ureteroscopy (ILY) in Laser Treatment of Nephrolithiasis in the Upper Urinary Tract
Verified date | August 2020 |
Source | Centre Hospitalier Universitaire de Nimes |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this pilot study, we wish to evaluate the performance of a robotic flexible ureteorscopy (ILY) in the treatment of nephrolithiasis in the superior excretory system
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | January 2020 |
Est. primary completion date | January 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - The patient must have given their free and informed consent and signed the consent form - The patient must be a member or beneficiary of a health insurance plan - The patient is at least 18 years old - The patient has a single kidney stone in the calyx or the pelvis between 5 and 15mm something to do with a JJ probe - Patient has an indication for in situ lithotripsy by supply ureteroscopy Exclusion Criteria: - The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study - The patient is under safeguard of justice or state guardianship - The subject refuses to sign the consent - It is impossible to give the subject informed information - The patient is pregnant or breastfeeding - Patient treated with anticoagulants - Documented untreated urinary infection within the previous 48 hours |
Country | Name | City | State |
---|---|---|---|
France | CHU Nimes | Nîmes |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire de Nimes |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of procedures performed entirely using the telemanipulator | end of study: 3 months | ||
Primary | Number of procedures where the surgeon had to switch to manual mode or dedock the device | end of study: 3 months | ||
Primary | If telemanipulator remained stable during procedure | Yes/no | end of procedure; less than 2 hours | |
Primary | Time of procedure | end of procedure; less than 2 hours | ||
Primary | Docking time | time between docking of device and use of gamepad | end of procedure; less than 2 hours | |
Primary | Time taken to track kidney stones | end of procedure; less than 2 hours | ||
Primary | Time taken for complete exploration of renal cavities | end of procedure; less than 2 hours | ||
Primary | Laser fragmentation time | end of procedure; less than 2 hours | ||
Primary | Speed of fragmentation | mm3/minute | end of procedure; less than 2 hours | |
Primary | Any joint pain strain experienced by the surgeon before and after intervention | binary yes/no | end of procedure; less than 2 hours | |
Primary | Satisfaction of surgeon in using the device | Custom-made questionnaire with 3 sections measuring: ease of use, ergonomics in exploration of renal cavities and stability during fragmentation of laser | end of procedure; less than 2 hours | |
Secondary | Describe the rate of intra-operative complications during procedure | end of procedure; less than 2 hours | ||
Secondary | Describe the rate of intra-operative complications | 1 month | ||
Secondary | Integrity of the ureroscope at the end of the procedure | binary yes/no | end of procedure; less than 2 hours |
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