Effectiveness of Cranberry Ingestion on Bacterial Adhesion: An Adjunct Study
Primary Purpose
Asymptomatic Bacteriuria
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cranberry Juice
De-Activated Cranberry juice
Sponsored by
About this trial
This is an interventional other trial for Asymptomatic Bacteriuria focused on measuring Pregnancy, Cranberry, Asymptomatic Bacteruria
Eligibility Criteria
Inclusion Criteria:
- Intrauterine pregnancy
- Documented fetal viability (either by fetal heart tones present by Doppler auscultation, or by ultrasonic visualization of cardiac motion
- Estimated gestational age by last menstrual period and/or by ultrasonographic fetal measurements of 16 weeks or less
Exclusion Criteria:
- Exclusion criteria will include:
- Suspected non-viable or ectopic gestation
- Patient desires pregnancy termination
- Significant underlying medical complication, such as chronic hypertension, insulin-requiring diabetes, chronic renal failure, cardiac disease, sickle cell disease, etc.
- Maternal age less than 18 years
- Patient is currently on or has received within the two weeks prior to enrollment antimicrobial therapy for reasons other than urinary tract infection.
Sites / Locations
- University of California, Irvine Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Cranberry 2xday
Cranberry + Placebo
Placebo 2xday
Arm Description
Cranberry juice (C) two times daily, a.m. and p.m.
De-Activated Cranberry juice in the am, then placebo (P) in the pm
Placebo in the form of juice two times daily in the a.m. and p.m.
Outcomes
Primary Outcome Measures
Antimicrobial Activity of Urine From Pregnant Subjects Following Cranberry Juice Cocktail (CJC)
The primary outcome measure was the measurement of bacteriuria in study subject urine, defined as having a urine culture with 100,000 or more of a single uropathogen (measured as cfu per ml).
Secondary Outcome Measures
Full Information
NCT ID
NCT00506025
First Posted
July 24, 2007
Last Updated
November 17, 2017
Sponsor
University of California, Irvine
1. Study Identification
Unique Protocol Identification Number
NCT00506025
Brief Title
Effectiveness of Cranberry Ingestion on Bacterial Adhesion: An Adjunct Study
Official Title
Effectiveness of Cranberry Ingestion on Bacterial Adhesion: Adjunct to Pilot Study of Daily Cranberry Ingestion of Cranberry Juice for the Prevention of Asymptomatic Bacteriuria in Pregnancy
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
February 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Irvine
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is to help determine if drinking cranberry juice can decrease risk for asymptomatic bacteriuria (ASB). ASB occurs when there are bacteria in the urine without any symptoms. It will also see if there is a difference in this effect between pregnant and non-pregnant women.This research project is also designed to see what happens to bacterial binding to the lining of the bladder after drinking cranberry juice when special problems occur with pregnancy such as diabetes (a sugar metabolism problem) or ASB is already occurring.
Detailed Description
This study is an adjunct to a proposal the premise of which is daily cranberry ingestion during pregnancy may be an effective preventative approach to development of asymptomatic bacteriuria (ASB), a condition which predisposes to both preterm birth and upper urinary tract infection. We proposed to NCCAM a pilot randomized, controlled trial (RCT) in which pregnant women beyond 12 weeks' gestational age will be assigned to one of three schedules for cranberry ingestion: Group A will consume cranberry juice twice a day with breakfast and dinner; Group B will consume cranberry juice at breakfast followed by placebo at dinner; and Group C will consume placebo with meals. Both the cranberry juice and placebo will be of scientific grade, provided by an NIH-contractor. Both are well-characterized, presenting a low-carbohydrate load and low-calorie content per dose (40 cal per 8 oz. dose). Our intent is to 1) generate data comparing the frequency of asymptomatic bacteriuria in pregnant women consuming cranberry juice daily versus placebo, and to 2) create the infrastructure to complete this pilot study and to gather sufficient data to support an R01 for a larger, multi-center RCT focused on the prevention of ASB in pregnancy with daily cranberry juice ingestion.
The reviewers of our proposal enumerated specific weaknesses including 1) a need to evaluate urine from cranberry treated patients, and 2) consideration of bacterial virulence/adherence. The additional variable of gestational diabetes also received comment from the reviewers, and we acknowledge that predisposition in the Hispanic population to this obstetrical complication could impact results. A constituent of cranberries is fructose, which has been implicated in the inhibition of E. coli with type 1 fimbriae (mannose-sensitive) (2). We hypothesize that the glucosuria associated with diabetes in pregnancy may influence the effectiveness of cranberry to prevent asymptomatic bacteriuria.
We must address these weaknesses to strengthen chances for continued funding and competitive renewal.
We have made inquiries with other researchers, and have discovered no direct urine or serum assays by which to measure cranberry metabolites. We understand that there is an R21 proposal under consideration to develop a urinary assay for this purpose under the same RFA. Amy Howell, PhD, of the Marucci Center for Blueberry/Cranberry Research of Rutgers University, one of the field's foremost researchers in this field, and others have indirectly assayed compliance to cranberry by evaluating adherence of piliated E. coli strains before and after cranberry exposure (1). In response to the recent call for proposals for faculty research from the UCI Committee on Research, I proposed this pilot study in collaboration with Dr. Howell.
In this proposal, we will collect the urine from various participants in the R21 trial so as to characterize the effect of cranberry juice ingestion on bacterial adherence. We will ask women to collect their urine for a four-hour time period including first-morning void. The urine samples will be sent to Dr. Howell's laboratory at Rutgers University for analysis. We will collect urine from pregnant women who are assigned to cranberry and to placebo, and from those women who develop bacteriuria following cranberry and following placebo ingestion. We also plan to identify a group of reproductive age, healthy, and non-pregnant women to ingest the active cranberry product or placebo for three days, and on the third day, collect a four-hour timed sample in the same manner as the pregnant women in our control group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asymptomatic Bacteriuria
Keywords
Pregnancy, Cranberry, Asymptomatic Bacteruria
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
51 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cranberry 2xday
Arm Type
Active Comparator
Arm Description
Cranberry juice (C) two times daily, a.m. and p.m.
Arm Title
Cranberry + Placebo
Arm Type
Active Comparator
Arm Description
De-Activated Cranberry juice in the am, then placebo (P) in the pm
Arm Title
Placebo 2xday
Arm Type
Placebo Comparator
Arm Description
Placebo in the form of juice two times daily in the a.m. and p.m.
Intervention Type
Dietary Supplement
Intervention Name(s)
Cranberry Juice
Intervention Description
Low-calorie, Low-carbohydrate content 8 oz dose of Cranberry juice
Intervention Type
Dietary Supplement
Intervention Name(s)
De-Activated Cranberry juice
Intervention Description
De-Activated Cranberry juice in the am, then placebo (P) in the pm
Primary Outcome Measure Information:
Title
Antimicrobial Activity of Urine From Pregnant Subjects Following Cranberry Juice Cocktail (CJC)
Description
The primary outcome measure was the measurement of bacteriuria in study subject urine, defined as having a urine culture with 100,000 or more of a single uropathogen (measured as cfu per ml).
Time Frame
7 months, from enrollment at 3 months of pregnancy to delivery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Intrauterine pregnancy
Documented fetal viability (either by fetal heart tones present by Doppler auscultation, or by ultrasonic visualization of cardiac motion
Estimated gestational age by last menstrual period and/or by ultrasonographic fetal measurements of 16 weeks or less
Exclusion Criteria:
Exclusion criteria will include:
Suspected non-viable or ectopic gestation
Patient desires pregnancy termination
Significant underlying medical complication, such as chronic hypertension, insulin-requiring diabetes, chronic renal failure, cardiac disease, sickle cell disease, etc.
Maternal age less than 18 years
Patient is currently on or has received within the two weeks prior to enrollment antimicrobial therapy for reasons other than urinary tract infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deborah A Wing, MD
Organizational Affiliation
University of California, Irvine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, Irvine Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effectiveness of Cranberry Ingestion on Bacterial Adhesion: An Adjunct Study
We'll reach out to this number within 24 hrs