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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05376670
Other study ID # nWMODIV2_2022013
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 20, 2022
Est. completion date March 7, 2023

Study information

Verified date March 2023
Source Leiden University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Antimicrobial prophylactic treatment of recurrent UTI is limited by emerging resistance, antibiotic allergies and intolerances. Intravesical aminoglycoside instillations (IAI) have been shown to reduce recurrence rate, without a short-term decline in kidney function or hearing. Thus far, treatment satisfaction has not yet been assessed, while this may play an important role in treatment adherence and persistence. Moreover, there is no data on the long-term safety of IAI, e.g. regarding the development of (pre)malignant bladder lesions.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date March 7, 2023
Est. primary completion date March 7, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years - Currently receiving or having received (no minimal duration) continuous or post-coital IAI (gentamicin, tobramycin or amikacin) for recurrent UTI prophylaxis and treatment Exclusion Criteria: - Exclusively receiving IAI for 'on-demand' treatment of UTI and not prophylactic purposes - Receiving IAI as suppressive therapy for chronic prostatitis - Presence of a chronic indwelling catheter - Patient has objected to the use of his/her data - Inability to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Intravesical aminoglycoside instillations
Overnight instillation of an aminoglycoside (CIC), varying treatment regimens

Locations

Country Name City State
Netherlands Leiden University Medical Center Leiden South Holland

Sponsors (1)

Lead Sponsor Collaborator
Leiden University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Treatment satisfaction regarding intravesical aminoglycoside instillations (IAI) Measured with Treatment Satisfaction Questionnaire for Medication version II (TSQM-II), value ranging from 0 to 100 (with a score of 100 indicating the highest treatment satisfaction) 1 year
Secondary Time to first UTI recurrence after initiation of IAI First 6 months of IAI
Secondary Number of UTI recurrences First 6 months of IAI
Secondary Number of UTI recurrences that are treated with IAI alone (no systemic antimicrobial therapy) First 6 months of IAI
Secondary Number of patients that wish to (dis)continue IAI 6 months after initiation of IAI
Secondary Proportion of patients that have a UTI episode caused by the same MDRO uropathogen as before start of IAI 6 months after initiation of IAI
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