ClinicalTrials.Veeva

Menu

Measurement of Urinary Catabolites of PACs as Biomarkers of Consumption of Cranberry Extracts (CUPACS)

L

Laval University

Status and phase

Completed
Phase 1

Conditions

Urinary Tract Infections

Treatments

Dietary Supplement: Cranberry extract

Study type

Interventional

Funder types

Other

Identifiers

NCT02087735
PACS-2013-SD

Details and patient eligibility

About

The purpose of this cross over pilot study is to investigate the urinary catabolites of Proanthocyanidines (PACs) as biomarkers of cranberry extracts in healthy young women.

Enrollment

15 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy women.
  • 18 to 40 years.

Exclusion criteria

  • No internet access.
  • No refrigerator access during the 9 hours of sample collection.
  • Women who had or expect to take antibiotic.
  • Women who had or expect to take cranberries, blueberries or bilberries in the form of berries, juice or extracts.
  • Women who had or expect to take dark chocolate.
  • Women who had personal history of acute or chronic renal failure.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

15 participants in 3 patient groups, including a placebo group

cranberry extract 1
Experimental group
Description:
One capsule with a proanthocyanidin standardized cranberry extract of 36 mg and one capsule of placebo cranberry extract.
Treatment:
Dietary Supplement: Cranberry extract
cranberry extract 2.
Experimental group
Description:
Two capsules with a proanthocyanidin standardized cranberry extract of 36 mg.
Treatment:
Dietary Supplement: Cranberry extract
cranberry extract 3.
Placebo Comparator group
Description:
Two capsules with a proanthocyanidin standardized cranberry extract of 2 mg.
Treatment:
Dietary Supplement: Cranberry extract

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems