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Flexible UreteroscopyNCT05633030

Ureteral Access Sheath or Percutaneous Nephrostomy During Flexible Ureteroscopy: Which is Better?

A study testing using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopy in people with Flexible Ureteroscopy, run by Benha University.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

we aim to compare the safety and efficacy of flexible ureteroscopy with ureteral access sheath (group A) in comparison with flexible ureteroscopy without UAS but with PCN insertion (group B) either intra or post operaively by recording all data and the benefits , also comparing the drawbacks on each group Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Flexible Ureteroscopy
What is being tested?
using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
No sites listed yet
Study dates
1 Dec 2022to Jul 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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • patients with upper ureteric stones and mild hydronephrosis or renal pelvic stones less than 20 mm with mild hydronephrosis

Who cannot join

  • patients with active urinary tract infection and patients with uncontrolled coagulable status

Trial locations and contacts

No sites are listed yet.

mohamed abdrahman alhefnawy, assistant professor contact

00201003481084

dr.mohamedalhefnawy@gmail.com

hosam abdelfatah aboelnasr, lecturer contact

00201286296939

hosamabuelnasr@gmail.com

About this study

we aim to compare the safety and efficacy of flexible ureteroscopy with ureteral access sheath (group A) in comparison with flexible ureteroscopy without UAS but with PCN insertion (group B) either intra or post operaively by recording all data and the benefits , also comparing the drawbacks on each group

Read the detailed description

A prospective randomized controlled study will be conducted at benha university hospitals on adult patients with renal and, or upper ureteric stones which will meet the inclusion criteria will participate in the study comparing usage of ureteral access sheath and percutaneous nephrostomy during flexible ureteroscopy. After filling out the informed consent form, patients will be randomly assigned to one of the two groups.

Group A: 50 patients will be operated using UAS during flexible ureteroscopy. Group B: 50 patients will be operated using PCN during flexible ureteroscopy.

Inclusion/Exclusion criteria:

Inclusion criteria consists of adult patients with upper ureteric stones and mild hydronephrosis or renal pelvic stones less than 20 mm with mild hydronephrosis.

Exclusion criteria include patients with active urinary tract infection and patients with uncontrolled coagulable status.

All patient demographics regarding age, gender, body mass index and comorbidities will be recorded. History, physical examination and laboratory investigations are done to exclude active urinary tract infection. Noncontrast computed tomography of the abdomen and plain abdominal radiography, so data revealed as stone side, stone burden, number of stones, hydronephrosis with its grade and Hounsfield Unit.

Technique

Group A: flexible ureteroscopy and UAS. Patients will be placed in the lithotomy position under general anesthesia and given appropriate antibiotic cover. The bladder and ureteric orifice will be directly visualized by rigid cystoscopy prior to the introduction of a safety guidewire., a semirigid ureteroscopy will be performed over a second working wire up to the pelvi-ureteric junction (PUJ) or as far proximally as safely achievable, allowing passive dilatation of the ureteric orifce and ureter. ureteral dilation using serial dilators is carried out if needed and up to 14 French (Fr). Two sizes of UAS were used: COOK Medical Flexor 12/14 French (Fr) (wider) and 9.5/11.5Fr (narrower). Appropriately sized UAS was then inserted over the wire and positioned just distal to the PUJ or below upper ureteric stone under fluoroscopic guidance. We then perform a flexible ureteroscopy using Olympus URF-V2 (8.5 Fr) flexible ureteroscope to inspect the proximal ureter if there is upper ureteric stone, renal pelvis, and calyces for the presence of stones. Irrigation with 0.9% saline solution via a pressure-infusing system. Next, Holmium laser lithotripsy with a holmium:YAG laser [20 W; Lumenis (UK) Ltd., Elstree, UK] using a 272 micron laser fiber (Lumenis, Inc.) is carried out and/or stone extraction with a basket device.

Group B: flexible ureteroscopy without UAS and insertion of PCN. Under general anesthesia in the supine position and given appropriate antibiotic, ultrasound guided 8 Fr PCN will be inserted trans papillary in the lower calyx of the kidney by an expert intervention radiologist. The bladder and ureteric orifice will be directly visualized by rigid cystoscopy prior to the introduction of a safety guidewire., a semi rigid ureteroscopy will be performed over a second working wire up to the pelviureteric junction (PUJ) or as far proximally as safely achievable, allowing passive dilatation of the ureteric orifice and ureter. ureteral dilation using serial dilators up to 10 Fr if needed. We then perform a flexible ureteroscopy using Olympus URF-V2 (8.5 Fr) flexible ureteroscope and complete procedure as described in the previous group and nephrostomy is open for irrigation and small dusted stone particles get its way out. At the end of the procedure, a double pigtail ureteral stent is left for 14 days. Once the operation is finished, PCN will be closed for 1 day and then the PCN catheter will be removed.

Operative time, intra-operative complications (bleeding, perforation, incompletion of procedure) and hospitalization periods will be recorded. Our follow-up protocol consisted of urinalysis, serum creatinine, and noncontrast computed tomography in the first month after the operation to assess stone-free rates and ureteral stricture formation, elevated serum creatinine level, and UTIs in the follow-up period. We will define success as the absence of any residual stones in the kidney or stone fragments less than 2 mm. Evaluation for success will be at 1 month and 3 months after the procedure.

Data management and analysis Quantitative data will be expressed as mean and standard deviation. Qualitative data will be expressed as frequencies and percent. Independent t-test will be used to assess the statistical significance of the difference between two study groups mean. Chi square test will be used to examine the relationship between qualitative data. The p <0.05 is considered significant in all tests. All statistics will be carried out using SPSS version 24 for Windows.

References

  1. Donaldson JF, Lardas M, Scrimgeour D, Stewart F, MacLennan S, Lam TB, et al. Systematic review and meta-analysis of the clinical effectiveness of shock wave lithotripsy, retrograde intrarenal surgery, and percutaneous nephrolithotomy for lower-pole renal stones. Eur Urol. 2015;67:612-6.
  2. Bozkurt OF, Resorlu B, Yildiz Y, Can CE, Unsal A. Retrograde intrarenal surgery versus percutaneous nephrolithotomy in the management of lower-pole renal stones with a diameter of 15 to 20 mm. J Endourol. 2011; 25:1131-5.
  3. Pietrow PK, Auge BK, Delvecchio FC et al (2002) Techniques to maximize flexible ureteroscope longevity. Urology 60:784-788.
  4. Gorin MA, Santos Cortes JA, Kyle CC et al (2015) Initial clinical experience with use of ureteral access sheaths in the diagnosis and treatment of upper tract urothelial carcinoma. Urology 78(3):523-527.
  5. Guzelburc V, Guven S, Boz MY et al (2016) Intraoperative evaluation of ureteral access sheath-related injuries using post-ureteroscopic lesion scale. J Laparoendosc Adv Surg Tech A 26(1):23-26.
  6. De Coninck, V.; Keller, E.X.; Rodriguez-Monsalve, M.; Audouin, M.; Doizi, S.; Traxer, O. Systematic review of ureteral access sheaths: Facts and myths. BJU Int. 2018, 122, 959-969.
  7. Huang, J.; Zhao, Z.; AlSmadi, J.K.; Liang, X.; Zhong, F.; Zeng, T.; Wu, W.; Deng, T.; Lai, Y.; Liu, L.; et al. Use of the ureteral access sheath during ureteroscopy: A systematic review and meta-analysis. PLoS ONE 2018, 13, e0193600.
  8. Traxer O, Thomas A (2013) Prospective evaluation and classification of ureteral wall injuries resulting from insertion of a ureteral access sheath during retrograde intrarenal surgery. J Urol 189:580-584.
  9. Wright A, Williams K, Somani B et al (2015) Intrarenal pressure and irrigation flow with commonly used ureteric access sheaths and instruments. Cent Eur J Urol 68(4):434-438.
  10. Goodwin WE, Casey WC, Woolf W. Percutaneous trocar (needle) nephrostomy in hydronephrosis. J Am Med Assoc 1955;157: 891-4.
  11. Bell DA, Rose SC, Starr NK, Jaffe RB, Miller FJ Jr. Percutaneous nephrostomy for nonoperative management of fungal urinary tract infections. J Vasc Interv Radiol 1993;4:311-5
  12. Mokhmalji H, Braun PM, Martinez Portillo FJ, Siegsmund M, Alken P, Kohrmann KU. Percutaneous nephrostomy versus ureteral stents for diversion of hydronephrosis caused by stones: a prospective, randomized clinical trial. J Urol 2001;165:1088-92
  13. Lyncha MF, Ansona KM, Patelb U. Percutaneous nephrostomy and ureteric stent insertion for acute renal deobstruction consensus based guidance. J Clin Urol 2008;1:120-5.
Being tested
using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopy
Keywords
ureteral access sheath, ultrasound guided PCN

What participants receive

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

  • using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopyProcedure or surgery

    under general anesthesia and given appropriate antibiotic cover. a clssic flexible ureteroscopy procedure is done and appropriately sized UAS was then inserted over the wire and positioned just distal to the PUJ or below upper ureteric stone under fluoroscopic guidance. We then perform a flexible ureteroscopy using Olympus URF-V2 (8.5 Fr) flexible ureteroscope to inspect the proximal ureter if there is upper ureteric stone, renal pelvis, and calyces for the presence of stones. Irrigation with 0.9% saline solution via a pressure-infusing system. Next, Holmium laser lithotripsy with a holmium:YAG laser [20 W; Lumenis (UK) Ltd., Elstree, UK] using a 272 micron laser fiber (Lumenis, Inc.) is carried out and/or stone extraction with a basket device, in the other group we add inserted trans papillary in the lower calyx of the kidney by an expert intervention radiologist

Study groups in NCT05633030
Study groupRoleWhat they receive
operated using UAS during flexible ureteroscopyActive comparatorNot described
Receives: Procedure: using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopy
operated using PCN during flexible ureteroscopyActive comparatorNot described
Receives: Procedure: using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopy

What is being measured

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

  1. intra-operative complications

    Operative time, intra-operative complications (bleeding, perforation, incompletion of procedure) and hospitalization periods

    Measured: 3 mothes

Timeline

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

  1. First posted1 Dec 2022
  2. Study start1 Dec 2022 (estimated)
  3. Primary completionJun 2023 (estimated)
  4. Study completionJul 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
Group A: 50 patients will be operated using UAS during flexible ureteroscopy. Group B: 50 patients will be operated using PCN during flexible ureteroscopy.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05633030
Sponsor's protocol ID
Ureteral access sheath or PCN
Status last verified
Nov 2022
First submitted
21 Nov 2022
Last updated
2 Dec 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing using UAS during flexible ureteroscopy and using PCN during flexible ureteroscopy in people with Flexible Ureteroscopy, run by Benha University.

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 1 inclusion and 1 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 2 Dec 2022. Status can change between updates, so confirm with the study contact before making plans.

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?

Contact mohamed abdrahman alhefnawy, assistant professor (00201003481084, dr.mohamedalhefnawy@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

intra-operative complications (time frame: 3 mothes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 2 Dec 2022.

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