Nephrolithiasis Clinical Trial
— HOTLaserOfficial title:
Comparison of Lumenis Pulse 120H Moses 2.0 Holmium Laser vs. Olympus Soltive Thulium Fiber Laser for Mini-percutaneous Nephrolithotomy
Verified date | February 2024 |
Source | MaineHealth |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a single institution, single surgeon, randomized controlled trial to evaluate the Boston Scientific Lumenis Pulse 120H Moses 2.0 holmium laser versus the Olympus Soltive Superpulsed thulium fiber laser (TFL) for medium-to-large stones in the mini PCNL setting.
Status | Enrolling by invitation |
Enrollment | 52 |
Est. completion date | June 1, 2027 |
Est. primary completion date | June 1, 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years to 90 Years |
Eligibility | Inclusion Criteria: - Scheduled to undergo mini PCNL for nephrolithiasis - Stone burden (multiple stones acceptable) with largest stone 1cm - 3 cm in greatest dimension on bone window of noncontrast CT within a 6 month preoperative period. - Able to give informed consent - Age 21 or older Exclusion Criteria: - Patients scheduled to undergo concurrent non-PCNL procedure such as contralateral ureteroscopy - Inability to give informed consent - Age less than 21 - Body Mass Index (BMI) >45 - Pregnant or breastfeeding patients - Stone burden outside of inclusion criteria range - Untreated urinary tract infections - Uncontrolled bleeding disorder and coagulopathy - Abnormal upper tract anatomy such as presence of ureteral strictures or complete ureteropelvic junction (UPJ) obstruction - Patients with urinary diversion such as ileal conduit or neobladder - Any preexisting medical condition or situation that, in the investigator's opinion, could put the participant at significant risk, confound the study results, or interfere significantly with the participants' participation in the study - Are currently prescribed buprenorphine or methadone, or carry active diagnosis of chronic opioid use disorder |
Country | Name | City | State |
---|---|---|---|
United States | Maine Medical Center | Portland | Maine |
Lead Sponsor | Collaborator |
---|---|
MaineHealth | Boston Scientific Corporation |
United States,
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Length of stay | Length of stay in hospital after procedure. | 0-72 hours following procedure | |
Other | Safety Profile and Adverse Events | Loss of blood during the procedure, immediate and delayed complications, subsequent stone events, emergency department visits. | The duration of the operation and 90 days post procedure | |
Other | Subjective pain scores | Mean and worst pain scores on the numerical rating scale (NRS) postoperatively and at time of discharge. Numerical rating scale is reported as integers 0-10, with 10 being the worst pain intensity. | Immediately postoperatively through stent removal (0-14 days) | |
Primary | Laser Treatment Time | Measured in minutes and seconds. Total laser treatment time will be total cumulative lasing time. | The duration of the procedure | |
Secondary | Retreatment rate | Participants undergoing ureteroscopy, shockwave lithotripsy or repeat percutaneous stone treatment for the same stone(s) within 90 days. | 90 days | |
Secondary | Total Operative Time | The time the procedure takes, starting at time of instrument insertion after positioning and draping and end at instrument removal. | The duration of the operation | |
Secondary | Stone-Free Rate | No fragments greater than 3 mm in greatest dimension measured on low-dose noncontrast CT imaging approximately 8-12 weeks after surgery. | 8-12 weeks after surgery |
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