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Probiotics as a Prophylactic Aid in Women With Recurrent Urinary Tract Infections (UTI's)

Not Applicable
Conditions
Urinary Tract Infections
Interventions
Dietary Supplement: UREX-cap-5
Dietary Supplement: Placebo Y cap G-3
Registration Number
NCT00781625
Lead Sponsor
University Hospital, Akershus
Brief Summary

To investigate if administration of probiotics, either orally or vaginally,

* Can reduce the number of episodes of acute bacterial cystitis and/or

* Has tolerable adverse effect profile

* Improves general QoL in these women

* Improves the immune function and other physiological stress markers

* Reduces inflammation in urinary bladder epithelium

Detailed Description

Chronic recurrent bacterial cystitis is a condition that is disabling to a great extent and which influences quality of life and freedom of movement. The episodes can be painful, and lead to extensive use of antibiotics, which in itself promotes development of bacterial strains increasingly resistant to antibiotics, but do not prevent relapses. Almost all cystitis' in women are ascending infections from bacteria in the vagina, following colonization from the rectum. There have, however, been reported indications that there may be bacteria colonies within the urothelium that might give rise to relapses of the infections, rather than pure reinfection from ascending pathogens.

Probiotics are cultures of viable microorganisms, which show a positive effect on the general condition of the host when administered. Among the lactic acid bacteria (LAB), lactobacilli are the most commonly used for probiotics, and they have an excellent safety record. In terms of UTI, weekly or twice weekly intravaginal instillation of Lactobacillus strains GR-1 and B-54 have led to reduced recurrences. This concept has been supported by a 2006 pilot study showing that intravaginal administration of Lactobacillus crispatus GAI 98322 every two days for one year, had the potential to reduce the UTI recurrences. Another approach has been taken whereby lactobacilli are administered orally with a view of simulating how the pathogens reach the vagina. The studies have shown that L. rhamnosus GR-1 and L. reuteri (formerly fermentum) RC-14 can reach the vagina after daily oral ingestion, and they can lower the bacterial and yeast pathogen numbers.

The aim of the study is to try to normalize the vaginal bacteriological milieu so that the more pathogenic subpopulation of bacteria strains are displaced and are less likely to cause UTI.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
120
Inclusion Criteria
  • women 18-70 years old
  • spontaneous urination
  • > 3 UTI's previous year
  • no ongoing prophylactic antibiotic treatment
Exclusion Criteria
  • > 50 ml residual urine
  • neurological bladder disease
  • known neoplasia, kidney stone or urinary tract abnormalities
  • use og indwelling catheter
  • pregnancy
  • diabetes
  • infrequent voiding pattern
  • symptoms that indicate interstitial cystitis
  • creatinin > 250 micmol/L
  • participating in other clinical trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Probiotic oral capsulesUREX-cap-5Probiotic oral capsules, placebo vaginal capsules
Probiotic vaginal capsulesUREX-cap-5Probiotic vaginal capsule, placebo oral capsule
placeboPlacebo Y cap G-3placebo oral capsule, placebo vaginal capsule
Primary Outcome Measures
NameTimeMethod
Reduction in number og episodes og lower UTI6 months intervention period
Improvement of QOL6 months intervention period
Secondary Outcome Measures
NameTimeMethod
Improvement of immune function6 months
Effects are non-dependant og nutritional status6 month2
Effects are non-dependant of known factors contributing til UTI's6 months
Decreases inflammation in the urinary bladder epithelium6 months
Normalizes vaginal microflora6 months

Trial Locations

Locations (2)

Akershus Universitetssykehus HF

🇳🇴

Lørenskog, Akershus, Norway

St.Olavs Hospital

🇳🇴

Trondheim, Norway

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