mannoseRUTIs: D Mannose for Prevention and Treatment of RUTIs

Sponsor
IRCCS Policlinico S. Matteo (Other)
Overall Status
Completed
CT.gov ID
NCT03790254
Collaborator
(none)
500
1
107.8
4.6

Study Details

Study Description

Brief Summary

The aim of this review is to address clinical reliability, efficacy and safety of long-term treatment with oral D Mannose for the prevention of recurrent urinary tract infections (RUTIs) in females.

Condition or Disease Intervention/Treatment Phase
  • Other: systematic review

Detailed Description

A comprehensive systematic MEDLINE, Embase, Cochrane search was performed for English language reports published before December 2018 using the term "recurrent urinary tract infections and d mannose." We searched Medline, Embase, and the Cochrane Register of Controlled Trials since January 2010 to December 2018. Eligible studies did not include non-oral therapy, local (vaginal) treatment in women with RUTIs.

Study eligibility criteria- We identified eligible original articles. The heterogeneity of the available studies, their different rationale and aim, the assumption of d mannose for prophylaxis or treatment of recurrent UTIs need to be taken into account.

Study Design

Study Type:
Observational
Actual Enrollment :
500 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Oral D Mannose in the Prevention and Treatment of Recurrent Urinary Tract Infections: a Systematic Review
Actual Study Start Date :
Jan 1, 2010
Actual Primary Completion Date :
Dec 20, 2018
Actual Study Completion Date :
Dec 25, 2018

Outcome Measures

Primary Outcome Measures

  1. research literature data on d mannose for prevention and treatment of recurrent urinary tract infections. [January 2010-December 2018]

    literature search of the Medline, Embase, and Cochrane Library databases

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

recurrent urinary tract infections (RUTIs)

Exclusion Criteria:

Upper urinary tract infections, severe clinical symptoms, fever > 37,5 with lumbar pain

Contacts and Locations

Locations

Site City State Country Postal Code
1 Urology Department Fondazione IRCCS Policlinico San Matteo Pavia Italy 27100

Sponsors and Collaborators

  • IRCCS Policlinico S. Matteo

Investigators

  • Principal Investigator: Daniele Porru, MD, Fondazione IRCCS Policlinico San Matteo

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Daniele Porru, MD, IRCCS Policlinico S. Matteo
ClinicalTrials.gov Identifier:
NCT03790254
Other Study ID Numbers:
  • ReviewUTIs
First Posted:
Dec 31, 2018
Last Update Posted:
Dec 31, 2018
Last Verified:
Dec 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Daniele Porru, MD, IRCCS Policlinico S. Matteo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 31, 2018