MedTrace Logo

Evaluation of Increased Absorption of a Curcumin Emulsion (CurQ+) in Healthy Volunteers

NCT04103788 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2021-12-13

No results posted yet for this study

Summary

This study is intended to evaluate the comparative effects of direct analysis of serum samples versus pre-treatment with enzymatic hydrolysis in split samples obtained from dosing with a highly absorbed curcumin emulsion product that is commercially available as BIOCURC.

Conditions

  • Bioavailability

Interventions

DIETARY_SUPPLEMENT

95% Curcuminoid Powder

1200 mg curcuminoids

DIETARY_SUPPLEMENT

CurQ+

400 mg curcuminoids + coconut oil + polysorbate

Sponsors & Collaborators

  • ESM Technologies, LLC

    lead INDUSTRY

Principal Investigators

  • Kevin J. Ruff, Ph.D. · Stratum Nutrition

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
21 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-03-27
Primary Completion
2018-04-14
Completion
2018-12-13

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04103788 on ClinicalTrials.gov