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Clinical Trials/NCT06022952
NCT06022952RecruitingNot Applicable

Randomized, Single Center Controlled Trial of the Effect of the "Stone MD" Mobile App on the Prevention of Forgotten Ureteral Stents in Patients With Urolithiasis

St. Petersburg State Pavlov Medical University3 sites in 1 country200 target enrollmentStarted: February 1, 2023Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
200
Locations
3
Primary Endpoint
Delayed stent removal
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The Impact of the "Stone MD" Mobile App on the Prevention of Forgotten Ureteral Stents

Detailed Description

Inclusion Criteria:

  1. Male and female patients aged 18 to 80 years who have a Ch 4.7-6.0 polyurethane ureteral stent

Exclusion Criteria:

  1. Active phase of urinary tract infection
  2. Insufficient level of social adaptation
  3. The patient does not have a smartphone with Internet access

All patients will be randomized into 2 groups:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Male and female patients aged 18 to 80 years who have a Ch 4.7-6.0 polyurethane ureteral stent

Exclusion Criteria

  • •Active phase of urinary tract infection
  • •Insufficient level of social adaptation
  • •The patient does not have a smartphone with Internet access

Outcomes

Primary Outcomes

Delayed stent removal

Time Frame: 30 days

Number of patients who delayed stent removal in both groups (less than 14 days)

Forgotten stent removal

Time Frame: 30 days

Number of patients who forgot to remove the stent in both groups (removed the stent more than 14 days from the expected date of removal)

Removed on time

Time Frame: 30 days

Number of patients who removed the stent on time in both groups

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
St. Petersburg State Pavlov Medical University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (3)

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