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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03344120
Other study ID # AOUCSSTURAB004
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 8, 2020
Est. completion date December 16, 2020

Study information

Verified date December 2020
Source Azienda Ospedaliera Città della Salute e della Scienza di Torino
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Double J ureteral stents (DJ) are widely used in urological practice and commonly inserted after most of ureteroscopies. Stent-related symptoms (SRS) represent a major issue. Many research lines have been explored with the aim of decreasing SRS: Vogt et al. projected a self-made pigtail suture stent (PSS) replacing the distal pigtail with a 0.3 Fr suture reaching the bladder, showing decreased SRS and good tolerance. To date, these promising results hasn't been confirmed by a prospective randomized controlled trial (RCT) involving a marketed PSS. Thus, we designed a prospective single-blind RCT to compare SRS caused by marketed PSS and conventional DJ after uncomplicated URS for stone treatment.


Recruitment information / eligibility

Status Completed
Enrollment 84
Est. completion date December 16, 2020
Est. primary completion date November 2, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - ureteral or renal stones < 2 cm needing treatment through semirigid or flexible URS and laser lithotripsy - stone-free procedure and absence of intraprocedural complications - WHO performance status 0-2 Exclusion Criteria: - significant residual fragments at the end of the procedure - intraprocedural complications (e.g. ureteral damage or stricture) - indwelling double J stent - acute kidney failure - urinary tract infection - urinary tract abnormalities - pathologies or medications potentially influencing voiding pattern and pain perception

Study Design


Intervention

Other:
Administration of USSQ Symptoms questionnaire after stent positioning
Administration of USSQ Symptoms questionnaire to patients with two different type of stents after ureteroscopy

Locations

Country Name City State
Italy AOU Città della Salute e della Scienza Turin

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliera Città della Salute e della Scienza di Torino

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Urinary Symptom Index Score to compare Urinary Symptom Index Score (sum of USSQ Urinary symptoms scores) of suture stent and double J group, 2 weeks after surgery. 14 days
Secondary USSQ domains' scores to compare USSQ domains' scores of suture stent and double J group, 2 weeks after surgery 14 days
Secondary USSQ domains' scores to compare USSQ domains' scores of suture stent and double J group, 2 days after surgery 2 days
Secondary USSQ single answers to compare USSQ single answers of suture stent and double J group, 2 weeks after surgery 14 day
Secondary USSQ single answers to compare USSQ single answers of suture stent and double J group, 2 days after surgery 2 days
Secondary 2 weeks USSQ domains' subscores adjusted for baseline to compare 2 weeks USSQ domains' subscores adjusted for baseline of suture stent and double J group 6 weeks
Secondary complications and adverse events to compare complications and adverse events of suture stent and double J group 2 weeks
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