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Clinical dosage and effectiveness Study of ShanStar® Cranberry supplement for Prevention and Treatment against women's Urinary Tract Infections

Completed
Conditions
rinary tract infection
Urological and Genital Diseases
Urinary tract infection
Registration Number
ISRCTN55813586
Lead Sponsor
ShanStar Biotech, Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
60
Inclusion Criteria

1. Age between the age of 18-50
2. Female gender
3. Healthy individual with 3 or more episodes of urinary tract infections per year
4. Able to complete the research study

Exclusion Criteria

1. Terminal diesease or dementia
2. Abstain from any cranberry, health food fruit extracts, anti-oxidants, vitamins, minerals and antibiotics for 2 weeks prior to participation in the study
3. Pregnancy
4. Urine catherisation within previous 2 weeks of study
5. Participants with history of diabetes, cardiovascular disease, symptoms of pyelonephritis and stones in the urinary tract
6. Sexually transmitted disease
7. Pyuria or bacteriuria on urinalysis or positive urine culture ( will be treated and wait 2 weeks to be eligible)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
At 1, 2, and 3 months, the participants will return to answer urinary tract symptoms questions and provide urine for complete urialysis and culture.<br>Primary outcome measures are:<br>1. Decrease in urinary tract infection symptoms score and decreased bacteriruia and pyuria and culture in urine study
Secondary Outcome Measures
NameTimeMethod
o secondary outcome measures
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