Osteoporosis Clinical Trials

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Blackcurrants Mitigate Postmenopausal Bone Loss Through Gut Microbiota-Bone Axis: A Randomized Clinical Trial Coupled With a Multi-Omics Approach to Inform Precision Nutrition

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The goal of this clinical trial is to evaluate the effects of blackcurrant (BC) supplementation on changes in bone density and gut microbiome composition in postmenopausal females.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 45
Maximum Age: 70
Healthy Volunteers: t
View:

• postmenopausal (defined as no more than 10 years since final menstrual cycle) females aged 45-70 years

• not on hormone replacement therapy for at least one year before initiation of the study

• maintaining normal exercise level (\< 7 hours/week) and willing to avoid exercise for 24 hours prior to blood and stool sampling

• willing to ingest a dietary blackcurrant supplement or placebo (up to 1,176 mg/day, three 392mg capsules)

• willing to avoid other dietary supplements for the duration of the study

• willing to avoid intake of foods extremely rich in anthocyanins and fermented dairy products containing viable Bifidobacteria or Lactobacilli

• willing to have three blood draws, three stool collections, and three bone scans

Locations
United States
Connecticut
University of Connecticut, Department of Nutritional Sciences
RECRUITING
Storrs
Contact Information
Primary
Ock Chun, PhD
ock.chun@uconn.edu
860-486-6275
Backup
Briana Nosal, MS
briana.nosal@uconn.edu
860-878-0679
Time Frame
Start Date: 2026-07
Estimated Completion Date: 2029-09
Participants
Target number of participants: 159
Treatments
Active_comparator: Low-BC Group
Low-dose BC extract
Active_comparator: High-BC Group
High-dose BC extract
Placebo_comparator: Control Group
Placebo (no BC extract)
Sponsors
Leads: University of Connecticut

This content was sourced from clinicaltrials.gov