Skip to content

The Effects of Oral Curcumin on Heme Oxygenase-1 (HO-1) in Healthy Male Subjects

The Effects of Oral Curcumin on Heme Oxygenase-1 (HO-1) in Healthy Male Subjects

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00895167
Acronym
CUMAHS
Enrollment
12
Registered
2009-05-08
Start date
2009-01-31
Completion date
2009-08-31
Last updated
2013-01-17

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

Conditions

Healthy

Keywords

Heme Oxygenase, Genetic Polymorphism, Healthy Subjects

Brief summary

Heme oxygenase 1 (HO-1) serves as a protective gene. Induction of HO-1 has therapeutic potential for several indications. The inducibility of HO-1 by curcumin will be evaluated in this pilot study. Furthermore, the influence of a modulating factor of HO-1 gene activity on the dinucleotide guanosine thymine repeat (GT) length polymorphism in the promotor region will be investigated.

Interventions

DIETARY_SUPPLEMENTcurcumin

one oral dose of 12 caplets = 12 g curcumin

Sponsors

Daniel Doberer
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Signed informed consent prior to any study-mandated procedure. * Male patient aged between 18 and 45 years (inclusive) at screening. * No clinically significant findings on the physical examination at screening. * Body mass index (BMI) between 18 and 28 kg/m2 (inclusive) at screening. * 12-lead ECG without clinically relevant abnormalities at screening. * Hematology, clinical chemistry, and urinalysis test results not deviating from the normal range to a clinically relevant extent at screening. * Negative results from urine drug screen at screening. * Ability to communicate well with the investigator, in the local language, and to understand and comply with the requirements of the study.

Exclusion criteria

* Known hypersensitivity to the study drug or any excipients of the drug formulation. * Treatment with another investigational drug within 3 weeks prior to screening. * History or clinical evidence of alcoholism or drug abuse within the 3-year period prior to screening. * History or clinical evidence of any disease and/or existence of any surgical or medical condition, which might interfere with the absorption, distribution, metabolism or excretion of the study drugs. * Smoking within the last 3 months prior to screening. * Previous treatment with any prescribed or OTC medications (including herbal medicines such as St John's Wort) within 2 weeks prior to screening. * Regularly intake of curcumin rich food * Loss of 250 ml or more of blood within 3 months prior to screening. * Positive results from the hepatitis serology, except for vaccinated subjects, at screening. * Positive results from the HIV serology at screening. * Presumed non-compliance. * Legal incapacity or limited legal capacity at screening.

Design outcomes

Primary

MeasureTime frame
The maximal HO-1 mRNA expression and HO-1 protein level in PBMCs48 hrs

Secondary

MeasureTime frame
Increase of plasma bilirubin level48 hrs

Countries

Austria

Outcome results

None listed

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