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NCT02034890 Clinical Trial

Intravesical Instillation of Hyaluronic Acid to Decrease Incidence of Urinary Tract Infection

Urinary Tract Infection Clinical Trial

Official title:
Is Intra - Neobladder Installations of Hyaluronic Acid, Effective in Reducing Neobladder Orthotropic Reconstruction Post-operative Urinary Tract Infections?

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02034890
Other study ID # RMC-7350
Secondary ID
Status Withdrawn
Phase Phase 4
First received
Last updated
Start date July 2015

Study information
Verified date April 2016
Source Rabin Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Prospective trial which includes instillation of intravesical hyaluronic acid in an attempt to reduce the incidence of urinary tract infections in patients after orthotopic neobladder reconstruction.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients undergoing radical cystectomy and orthotopic neobladder reconstruction

Exclusion Criteria:

- patients <18 years and unwilling to participate in this study

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Hyaluronic Acid
intravesical instillation of 40 mg of hyaluronic acid in 6 specific time points: 1,2,3 and 4 weeks postoperatively (After radical cystectomy and orthotopic neobladder reconstruction) 2 and 3 months postoperatively

Locations
Country Name City State
Israel Urology department, Rabin Medical Center Petach Tiqva

Sponsors (1)
Lead Sponsor Collaborator
Rabin Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary positive urinary culture 6 months
Secondary urinary tract infection 6 months
See also
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