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Ideal Time IntervalNCT04575480

The Ideal Time Interval Between Repeated Shock Wave Lithotripsy Sessions For Renal Stones: A Randomized Controlled Trial

A study testing Shock Wave Lithotripsy for renal stone. in people with Ideal Time Interval, run by Mansoura University at 1 site in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

There is no consensus about the required time intervals between repeated SWL sessions applied for renal stones with some centers waiting for 3 days, others for one week and others up to one month to repeat lithotripsy. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Ideal Time Interval
What is being tested?
Shock Wave Lithotripsy for renal stone.
Could I receive a placebo?
No, everyone receives an active treatment
How many people
150 participants
Where
1 siteEgypt
Study dates
15 Jul 2020to 1 Jan 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • Contraindications to ESWL:
  • Uncontrolled Hypertension
  • Renal insufficiency
  • Diabetic patient
  • Coagulopathy
  • Morbid obesity
Show all 11Show fewer
  • Upper urinary tract obstruction
  • Active urinary tract infection
  • Previous surgical or SWL treatment of renal stones.
  • Congenital renal anomalies and solitary kidney
  • Pediatric patients (age <18 years).

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Urology and Nephrology Center

    Al Mansurah, Dakahlia Governorate, 35514

Other trials in Egypt

About this study

There is no consensus about the required time intervals between repeated SWL sessions applied for renal stones with some centers waiting for 3 days, others for one week and others up to one month to repeat lithotripsy. In the 2019 EUA guidelines stated that "There are no conclusive data on the intervals required between repeated SWL sessions. However, clinical experience indicates that repeat sessions are feasible (within 1 day for ureteral stones).

The intense use of ESWL currently, the lack of knowledge about acute lesions caused by re-treatment within a short time interval and the empirical way by which treatment is conducted, stimulated us to search for a precise answers to the question What the ideal time interval between SWL sessions in the treatment of renal stone patients should be.

Read more

This randomized controlled trial will be conducted at Urology and Nephrology Center in Mansoura, Egypt. Patients more than 18 years old with single primary renal stone fulfilling inclusion criteria will be randomly allocated to 3 groups (50 patients each).Group 1 will undergo SWL with 3 days between each session. Group 2 will undergo SWL with 7 days between each session and Group 3 will undergo SWL with 14 days between each session.

Study parameters will be renal damage including the following items:

  • Tubular damage will be assessed through estimation of changes in urinary excretion of renal tubular enzyme kidney injury molecule 1(KIM-1).
  • Glomerular damage will be assessed by estimation of proteinuria and changes in GFR calculated by renal isotope scan.
  • Renal morphological and haemodynamic changes.
  • Treatment success is defined as clinically insignificant residual fragments less than 4 mm size.
Read the detailed description

STUDY DESIGN:

Randomized Trial

STUDY SETTING/LOCATION:

The study will be conducted in a single tertiary center, Urology and Nephrology Centre in Mansoura, Egypt.

STUDY POPULATION:

Adults (>18years) with primary single renal stone amenable for SWL according to EUA guidelines (C. TÜRK, 2019) .

Inclusion criteria Adult patient with ≤ 2 cm single calyceal renal stone in a normal functioning kidney.

Exclusion criteria:

  1. Contraindications to ESWL:
  • Uncontrolled Hypertension
  • Renal insufficiency
  • Diabetic patient
  • Coagulopathy
  • Morbid obesity
  • Upper urinary tract obstruction
  • Active urinary tract infection
  1. Previous surgical or SWL treatment of renal stones.
  2. Congenital renal anomalies and solitary kidney
  3. Pediatric patients (age <18 years). STUDY GROUPS Patient fulfilling the study criteria will be randomly allocated to one of three groups (50 Patient in each): Group 1 will undergo SWL with 3 days between each session. Group 2 will undergo SWL with 7 days between each session and Group 3 will undergo SWL with 14 days between each session.

Each patient will serve as internal control through comparing both pre-ESWL and post-ESWL values of our study parameters. / Candidates Potential participants will be invited to participate in this study after signing an informed consent. Potential participants will be given enough information, in a way they will understand, about the potential risks and benefits of being involved in this clinical study.

Baseline evaluation (Before ESWL) (S0):

Complete history and physical examination. Laboratory Investigations

Blood Samples:

Blood sample will be withdrawn Pre-ESWL (B.S0) for:

  • CBC
  • Serum creatinine
  • Prothrombin concentration

Urine Samples:

  • Samples of urine will be obtained before ESWL session(U.S0) for Urine analysis \&estimation of KIM-1
  • Urine culture will be obtained in cases of pyuria

Radiological investigation:

  • NCCT will be performed. Stone criteria will be identified as regard to volumes, site, location, stone density and associated hydronephrosis.
  • I.V.P (intravenous pyelography) will be performed if needed to exclude the presence of narrow neck calyx or stones in closed calyces.
  • Dynamic renal scintigraphic scanning using technetium-99m Diethylene Triamine Pentaacetic Acid (TC-99m DTPA). The renal uptake, percentage of uptake from the injected dose, split function, ERPF, corrected glomerular filtration rate (GFR), time to peak clearance (T max), and half-time clearance will be calculated, because these parameters are helpful indicators in the evaluation of renal function.
  • Functional MRI assessment to evaluate the renal tissue oxygenation using Blood-Oxygen Level Dependent (BOLD) and possible anatomical changes

Randomization Randomization will be performed using computer generated, sequentially numbered method.

Procedure technique:

The following protocol will be applied for all patients in study groups. SWL will be performed using the Dornier Gemini lithotripter (Dornier MedTech, Wessling, Germany) . A total of 3 000 shocks will be delivered at 80 shocks/min. The patient will receive 1 mg/kg pethidine i.v. for analgesia. Treatment will begin at machine power step 1, which will deliver 49 MPa focal pressure and 0.35 mJ/mm2. Power will be gradually increased by one step for each 200 shocks up to step 4, which deliver 70 MPa and 0.7 mJ/mm2. The maximum session number will be 3 session. Patient treated with <2 sessions will be excluded from the analysis.

After 1st ESWL session:

  • Urine sample will be obtained 2to 4 hours after the end of the first session (U.S1) for estimation of urinary proteinuria and estimation of KIM-1
  • Visual analogue scale will be compared between the study groups
  • Non contrast spiral CT (low dose) will be performed before 2nd session to detect residual fragments, presence of obstruction and the need for re-treatment.
  • Functional MRI assessment to evaluate the renal tissue oxygenation.

After 2nd ESWL session:

  • Urine sample will be obtained after 2 to 4 hours after the second session (U.S2) for proteinuria and estimation of KIM-1.
  • Visual analogue scale.
  • Non contrast spiral CT (low dose will be performed before 3rd session to detect residual fragments, presence of obstruction and the need for re-treatment.
  • Functional MRI assessment to evaluate the renal tissue oxygenation.

After 3 months of the treatment :

  • Samples of urine will be obtained after 3 month from the start of treatment U.S3 for Urine analysis \& estimation of urinary proteinuria and estimation of KIM-1
  • Blood sample will be withdrawn (B.S3) for:
  • CBC
  • Serum creatinine and calculation of eGFR values
  • NCCT will be done after 3 months of the last session of ESWL for detection of the stone free rate.
  • Dynamic renal scintigraphic scanning using TC-99m DTPA as described before.
  • Functional MRI assessment to evaluate the renal tissue oxygenation Statistical analysis Analysis of data will be performed with Statistical Package for Social Science (SPSS) software. Continuous data will be presented as mean ± SD when normally distributed and as medium and range when non-normally distributed. Categorical data will be presented as frequency and percentage. Comparison between mean ± SD between the three groups will be carried out by ANOVA test. Comparison between the median and range between the 3 groups will be performed by Kruskal -Wallis test. Comparison between categorical variables between groups will be performed using Chi-square or Fisher Exact test as appropriate. Regression analysis to estimate the best model which can predict the related kidney injury. In all comparison, a P.value < 0.05 will be considered significant.
Being tested
Shock Wave Lithotripsy for renal stone.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Shock Wave Lithotripsy for renal stone.Procedure or surgery

    The following protocol will be applied for all patients in study groups. SWL will be performed using the Dornier Gemini lithotripter (Dornier MedTech, Wessling, Germany) . A total of 3 000 shocks will be delivered at 80 shocks/min. The patient will receive 1 mg/kg pethidine i.v. for analgesia. Treatment will begin at machine power step 1, which will deliver 49 MPa focal pressure and 0.35 mJ/mm2. Power will be gradually increased by one step for each 200 shocks up to step 4, which deliver 70 MPa and 0.7 mJ/mm2. The maximum session number will be 3 session. Patient treated with <2 sessions will be excluded from the analysis

Study groups in NCT04575480
Study groupRoleWhat they receive
Group 1Active comparatorGroup 1 will undergo SWL with 3 days between each session.
Receives: Procedure: Shock Wave Lithotripsy for renal stone.
Group 2Active comparatorGroup 2 will undergo SWL with 7 days between each session
Receives: Procedure: Shock Wave Lithotripsy for renal stone.
Group 3Active comparatorGroup 3 will undergo SWL with 14 days between each session.
Receives: Procedure: Shock Wave Lithotripsy for renal stone.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. to identify the ideal time interval between SWL sessions used for treatment of renal stones and subsequent renal damage.

    Renal damage:

    1. Tubular damage: Tubular damage will be assessed through estimation of changes in urinary execration of the renal tubular enzyme, Kidney injury molecule -1 (KIM-1).
    2. Glomerular damage: Glomerular damage will be assessed by the presence of proteinuria and changes of GFR calculated by renal isotope scan.
    3. Renal morphological and hemodynamic changes:
    • Changes will be assessed by estimation of ERPF by renal isotope scan.
    • The presence of peri-renal or subcapsular hematomas on non-contrast spiral CT.
    • Assessment of renal tissue oxygenation using functional MRI.

    Measured: 3 months

Secondary outcomes (1)
  1. 3 months stone free rate

    Treatment success is defined as clinically insignificant residual fragments of < 4 mm

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Oct 2020
  2. Study start15 Jul 2020
  3. Primary completion15 Jul 2022 (estimated)
  4. Study completion1 Jan 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized trial, conducted in Urology and Nephrology Centre in Mansoura, Egypt. Including adults \>18 years with primary single renal stone amenable for SWL according to EUA guidelines (≤ 2 cm single calyceal renal stone in a normal functioning kidney) . Exclusion criteria include contraindications to ESWL (uncontrolled Hypertension , coagulopathy etc), previous intervention for renal stones , congenital renal anomalies and solitary kidney. Patients will be randomized to one of three groups (50 Patient in each): Group 1 will undergo SWL with 3 days between each session , Group 2 will undergo SWL with 7 days between each session and Group 3 will undergo SWL with 14 days between each session. pre-ESWL and post-ESWL values will be compared.Participants will be invited after signing an informed consent including the potential risks and benefits of each intervention in this clinical study.
Masking
Single blind
Who is masked
Participant
Enrolment
150 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04575480
Sponsor's protocol ID
Urology and nephrology center
Status last verified
Oct 2020
First submitted
25 Sep 2020
Last updated
5 Oct 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
Yes: in partial fulfillment of MD Degree in urology

Publications

  • Fadallah M, Abdelhalim A, Hashem A, Mortada WI, Ibrahim HAM, Sheir KZ, Harraz AM, El-Kenawy MR, El-Nahas AR. The Ideal Interval Between Repeated Shockwaves Lithotripsy Sessions for Renal Stones: A Randomized Controlled Trial. J Endourol. 2023 Dec;37(12):1305-1313. doi: 10.1089/end.2023.0345.

    PubMed 37767632

Questions about this trial

What is this clinical trial studying?

A study testing Shock Wave Lithotripsy for renal stone. in people with Ideal Time Interval, run by Mansoura University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 5 Oct 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

to identify the ideal time interval between SWL sessions used for treatment of renal stones and subsequent renal damage. (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04575480, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Oct 2020.

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