Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03243682
Other study ID # Bidirectional SWL
Secondary ID
Status Active, not recruiting
Phase N/A
First received July 29, 2017
Last updated August 7, 2017
Start date September 1, 2016
Est. completion date March 1, 2018

Study information

Verified date July 2017
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

compare the outcomes of SWL for renal and upper lumbar ureteric stones using the alternating bidirectional approach versus the standard approach.


Description:

Shock wave lithotripsy (SWL) has been considered the preferred method for treating upper urinary tract stones since 1980s due to its minimally invasive characters and low morbidity. The overall stone free rates have been reported to be 80% to 90% .

In the presence of pregnancy, untreated urinary tract infection, decompensated coagulopathy, uncontrolled arrhythmia and abdominal aortic aneurysm, other treatment methods should be considered .

SWL is associated with some complications. The most common complications of SWL are renal colic (40%), gross hematuria (32%), urinary obstruction (30.9%), symptomatic bacteriuria (9.7%) and perirenal hematoma or subclinical subcapsular hematoma (4.6%).

There are many factors affecting the success of SWL as patient age, sex, body mass index (BMI), stone size, site and number, radiological renal features, congenital renal anomalies and presence of double-J (DJ) ureteric stent .

Regarding the renal stones, stones smaller than 10 mm had a success rate of 90%, while those larger than 10 mm had a success rate of 70%. Stones located in the renal pelvis and upper pole had a success rate of 87.3 and 88.5% respectively, while those located in the lower pole had a success rate of 69.5%. A single renal stone had a 78.3% success rate compared to 62.8% in multiple renal stones . Regarding the ureteric stones, stone size more than 10 mm was one of the strongest independent predictors of failure of SWL

Patients appear to have the best chance for successful SWL when they have small BMI and their stones are single and located in the renal pelvis . Skin to stone distance (SSD) measured by non-contrast computerized tomography scan (NCCT) has a significant role in the treatment of renal stones using SWL. Slow shock wave rate (60/min) is associated with increase in the success rate and decrease in pain, complication and number of session to achieve success when compared to rapid shock wave rate (120/min)

Some techniques were developed to increase the efficacy of SWL. In 1999, the bidirectional synchronous twin-pulse technique with variable angles between the shock wave reflectors was developed and it improved the quality and rate of stone disintegration in vitro and it was more effective than the traditional single generator and also it decreases the overall treatment times

The TWINHEADS 101 lithotripter comprises two identical under and over table reflectors to permit synchronous shock waves emission from two perpendicular directions to the same focal point. This technique intensifies and localizes the cavitations effects by the interacting focal zones of both reflectors, resulting in a better quality and rate of stone disintegration, especially with a right angle between the axes of the reflectors.

The first prospective clinical study was done in 2005 regarding synchronous twin-pulse SWL and it seems safe and effective for treating patients with renal and upper ureteric stones. The stone-free rate was 74% after one session and 100% after two sessions within a month

Based on the principle of the TWINHEADS lithotripter, we will use Dornier Gemini lithotripter to emit the shock waves from two different directions to the same focal point asynchronously for renal and upper lumbar ureteric stones.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 240
Est. completion date March 1, 2018
Est. primary completion date March 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient criteria:

1. Ability to give informed consent.

2. Normal laboratory profile as regarding serum creatinine, liver function, platelets count and prothrombin time.

- Stone criteria:

1. Single renal stone less than two cm or upper lumbar ureteric stone less than one cm.

2. Radio-opaque stones.

Exclusion Criteria:

1. Bleeding tendency.

2. Poor kidney function.

3. Pregnancy.

4. Abdominal aortic aneurysm.

5. Indwelling DJ ureteric stent or percutaneous nephrostomy tube (PCN).

6. Congenital anomalies of the urinary tract.

7. Untreated urinary tract infection.

8. Obstructed urinary tract distal to the stone.

Study Design


Intervention

Procedure:
Bidirectional Shock Wave Lithotripsy
the alternating bidirectional (under and over table) approach during SWL for renal and upper lumbar ureteric stones
Standard Shock Wave Lithotripsy
the standard unidirectional approach during SWL for renal and upper lumbar ureteric stones

Locations

Country Name City State
Egypt Urology and Nephrology center Mansoura

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary stone free rate three months after the last session residual less than 4 mm by non-contrast computerized tomography scan (NCCT) 18 months
Secondary severity of complications after SWL in both groups Clavien-Dindo scale of surgical complications 18 months
See also
  Status Clinical Trial Phase
Recruiting NCT06397287 - PROM Project Urology
Completed NCT03572348 - VeSpAR: Comparing Vessel-Sparing Anastomotic Repair and Transecting Anastomotic Repair in Isolated Short Bulbar Strictures. N/A
Completed NCT03339609 - Uroflow Measurement With Electromyography (EMG) to Identify Lower Urinary Tract Symptoms (LUTS): Conducted on Healthy Children N/A
Active, not recruiting NCT01529658 - Renal Hypothermia During Partial Nephrectomy N/A
Completed NCT05082142 - Tranexamic Acid to Improve Same-day Discharge Rates After Holmium Laser Enucleation of the Prostate (HoLEP) Phase 4
Completed NCT03668262 - ED50 of Cis-atracurium for Laryngeal Mask Incubation in General Anesthesia
Recruiting NCT04763538 - Quality and Outcome Measurements of Urological Patients
Completed NCT05032287 - Medical Expulsive Therapy Post-SWL For Renal Stones N/A
Not yet recruiting NCT03899298 - Safety and Clinical Outcomes With Amniotic and Umbilical Cord Tissue Therapy for Numerous Medical Conditions Phase 1
Recruiting NCT05169892 - Aquablation in Benign Prostatic Hyperplasia in Canada
Enrolling by invitation NCT03234543 - Remote Ischemic Conditioning in Abdominal Surgery N/A
Recruiting NCT05201131 - Canadian Cohort of Convective Thermal Therapy Using Rezūm System in Benign Prostatic Hyperplasia (BPH).
Recruiting NCT06187870 - Bank of Biological Material From Patients and Healthy Donors for the Study of Urological and Uro-oncological Pathologies
Completed NCT03847909 - A Study to Evaluate DCR-PHXC in Children and Adults With Primary Hyperoxaluria Type 1 and Primary Hyperoxaluria Type 2 Phase 2
Recruiting NCT04972890 - The Outcomes of Intracavernosal Umbilical Cord Mesenchymal Stem Cells Implantation in Patients With Diabetic Erectile Dysfunction Phase 2/Phase 3
Not yet recruiting NCT03258658 - Safety and Feasibility Study of Autologous Engineered Urethral Constructs for the Treatment of Strictures Phase 1
Terminated NCT02543645 - A Study of Varlilumab and Atezolizumab in Patients With Advanced Cancer Phase 1
Terminated NCT03843073 - Connected Catheter- Safety and Effectiveness Study N/A
Terminated NCT04826484 - Opioid Reduction Initiative During Outpatient Pediatric Urologic Procedures Using Exparel Phase 3
Terminated NCT04059159 - Connected Catheter - Safety and Effectiveness Study N/A