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Broccoli Supplement Dose Response

Broccoli Supplement Dose Response

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03399656
Enrollment
170
Registered
2018-01-16
Start date
2018-01-10
Completion date
2018-02-15
Last updated
2022-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Brief summary

Do daily high (4 tablets) or intermediate (2 tablets) administration of the broccoli-based dietary supplement Avmacol® have improved bioavailability over a broccoli sprout beverage rich in sulforaphane and its biogenic precursor, glucoraphanin? The beverage formulation has been used successfully in the investigators' previous intervention studies in regions of China with high levels of air pollution to reduce the body burden of carcinogenic and toxic pollutants. The investigators seek to evaluate a more stable, less expensive formulation of a broccoli sprout preparation that can be used for disease prevention in future studies.

Detailed description

The investigators will conduct a 3-armed placebo-controlled 16-day intervention with the dietary supplement Avmacol® to determine the bioavailability with repeated dosing of a simple tablet-based intervention in the study participants. As shown in Scheme 1, the 3 arms are: 1) 4 tablets of Avmacol® daily for 14 days; 2) 2 tablets of Avmacol® daily for 14 days together with 2 placebo tablets to maintain parity in consumption; and 3) 4 placebo tablets daily for 14 days. In addition, all participants will receive 4 placebo tablets for 2 consecutive run-in days prior to commencing intervention in the 3 distinct arms. Consecutive overnight (12-hour) urine samples will be collected during the 2-day run-in, the 14-day intervention and during a 5-day run-out period (total = 21 days). Additional day-time urine collections will be made at 2 timepoints: the day after administration of Avmacol® tablets begins and the day after the last administration of Avmacol® tablets. A blood sample will be collected at the beginning of the run-in and after the last Avmacol® dose (Day 17 for intervention groups, and for the placebo group) from each participant. The tablets will be taken before dinner each day.

Interventions

DIETARY_SUPPLEMENTAvmacol tablets

The active components of Avmacol® are ground broccoli seeds that provide glucoraphanin and freeze-dried broccoli sprouts that provide a stabilized form of the enzyme myrosinase, which converts glucoraphanin to sulforaphane.

DIETARY_SUPPLEMENTPlacebo tablets

MCC 90M Emcocel

Sponsors

Qidong Liver Cancer Institute
CollaboratorOTHER
Johns Hopkins Bloomberg School of Public Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Placebo control

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age ≥ 21 and ≤ 70 years who are residents of Qidong, China. 2. Able to provide written, informed consent. 3. Normal physical examination and medical history indicative of good general health with no history of chronic illness. 4. No hepatomegaly by clinical exam; 5. Normal liver function tests (ALT, aspartate aminotransferase (AST), bilirubin); 6. Normal renal function tests (creatinine, blood urea nitrogen (BUN), urinalysis); 7. Serum alpha-fetoprotein (AFP) negative.

Exclusion criteria

1. Pregnant (positive human chorionic gonadotropin (HCG) strip test) 2. Current or former diagnosis of cancer, with the exception of non-melanomatous skin cancer.

Design outcomes

Primary

MeasureTime frameDescription
Excretion of sulforaphane and metabolites in urineConsecutive overnight urine samples collected for the duration of the study (21 days)Levels of sulforaphane and its glutathione-conjugate derived metabolites will be measured in consecutive overnight urine samples

Secondary

MeasureTime frameDescription
Air pollution biomarkers in urineConsecutive overnight urine samples collected for the duration of the study (21 days)Levels of benzene mercapturic acid excreted in urine

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026