Trial Details

Not Recruiting
Basic Information
Clinical ID c2565
Identifier ACTRN12620000092998
Trial Title Single-arm pre-post study of 12 weeks duration investigating the effect of the Broth & Co Bone Broth powder on gastrointestinal disturbances in adults
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions lower gastrointestinal tract disorders;inflammatory bowel disease; lower gastrointestinal tract disorders inflammatory bowel disease;Oral and Gastrointestinal - Inflammatory bowel disease;Oral and Gastrointestinal - Normal oral and gastrointestinal development and function
Interventions Single-arm pre-post study of 12 weeks duration investigating the effect of the Broth & Co Bone Broth Powder on lower gastrointestinal disorders in adults. After a run-phase of 4 weeks serving as control phase, the intervention will comprise of 2 x 5g Bone Broth powder (2x 1 tsp from 100g pouch) mixed in 100-150 ml of warm water per day for 8 weeks. Participants will be supplied with 2x4 weeks of Bone Broth Powder for consumption. The commercially available Broth & Co Bone Broth freeze-dried powder is made from Australian grass fed and free range beef bone and connective tissue containing a nutrient rich mix of amino acids, minerals, collagen/gelatin and glucosamine/chondroitin. Compliance will be monitored by return of remaining investigational product at the end of the study.
Participant Information
Sponsor AProf Dr Karin Ried
City -
Country/Region Australia
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, ELDER, OLDER_ADULT
Study Design
Study Type Interventional
Phase Not Available
Time Information
Start Date 2025-04-24
Primary Completion Date -
Completion Date -