Skip to content

The Use of Direct Puncture Technique With Mini-PCNL

Single-center Randomized Study to Evaluate the Safety and Effectiveness of Direct Puncture of the Caliceal System in Minipercutaneous Nephrolithotripsy (Mini-PCNL)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04610840
Enrollment
60
Registered
2020-11-02
Start date
2020-07-01
Completion date
2022-04-01
Last updated
2021-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urolithiasis

Keywords

urolithiasis, PCNL, direct puncture

Brief summary

* A single-center randomized study to evaluate the safety and effectiveness of direct puncture of the caliceal system in mini-percutaneous nephrolithotripsy. * 60 patients * Inclusion criteria: 1. all patients aged 18 to 70 years who are planning mini-PCNL, ready to consent to the study 2. ASA scale 1-3 3. Solitary stone up to 2.5 cm 4. Single access to the caliceal system * Exclusion criteria: 1. Active infectious process 2. Coagulopathies 3. Abnormalities of the urinary system

Detailed description

All patients will be randomized into 2 groups: Direct puncture - patients who underwent directive puncture under ultrasound or Rg control. The number of patients is 30 people. Non-direct puncture - patients who underwent a PCS puncture with retrograde contrast. The number of patients is 30 people. Patients will be assigned a randomization number that matches their treatment. Block randomization using 10 blocks will be performed by a central randomization organization (www.randomize.net) using a computerized algorithm. Primary assessed indicators: 1. Gender 2. Age 3. Body mass index 4. Localization of the stone (side, pelvis, upper anterior cup, upper posterior cup, middle anterior cup, middle posterior cup, lower anterior cup, lower posterior cup) 5. Density of the stone 6. The presence of hydronephrosis Indicators assessed during the operation - will be assessed by the physician-researcher: 1. Installation of the ureteral catheter 2. Duration of puncture 3. Puncture method (ultrasound, X-ray) 4. The success of the insertion of a flexible guidewire into the calyceal system 5. Problems during dilation of the puncture course 6. Visualization (Excellent, Moderate, Poor) 7. Type of drainage (stent, nephrostomic tube) at the end of the operation Using the Visual Analogue Pain Scale (VAS), pain assessment is planned at 2 hours, 6 hours, 12 hours and 24 hours after surgery. In the postoperative period, the patient independently controls the intake of analgesics from the NSAID group (ketorolac 100 mg) (Patient-controlled analgesia). If the patient requires analgesics, the time of taking the drug will be recorded (pain relief on demand). Secondary Assessment: Postoperative Assessment 1. Complications (Clavien) 2. Hemoglobin level 24 hours after surgery 3. Creatinine level 24 hours after surgery 4. Assessment of Stone-Free status after surgery by performing multislice computed tomography of the kidneys and urinary tract without intravenous contrast

Interventions

PROCEDUREPuncture of the caliceal system

Puncture of the caliceal system under ultrasound/Xray control

Sponsors

St. Petersburg State Pavlov Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 to 70 years who are scheduled for mini-PCNL, ready to consent to the study * ASA scale 1-3 * Solitary kidney stone up to 2.5 cm * One access to the caliceal system

Exclusion criteria

* Active infectious process * Coagulopathies * Abnormalities of the urinary system

Design outcomes

Primary

MeasureTime frameDescription
Puncture durationduring the operation (mini-PCNL)Measurement of puncture duration (in seconds)
Number of patients with successful direct punctureduring the operation (mini-PCNL)Evaluation of efficacy
Purity of a visual intraoperative fieldduring the operation (mini-PCNL)Excellent, Moderate, Poor visualization
Body pain24 hours after operationUsing the Visual Analogue Pain Scale (VAS), pain assessment is planned at 2 hours, 6 hours, 12 hours and 24 hours after surgery

Countries

Russia

Contacts

Primary ContactDmitry S Gorelov
dsgorelov@mail.ru+79217964892
Backup ContactVladimir M Obidniak
v.obidniak@gmail.com+79218944746

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026