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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00402623
Other study ID # MEC 05.142.5
Secondary ID
Status Completed
Phase N/A
First received November 20, 2006
Last updated February 22, 2017
Start date January 2006
Est. completion date January 2006

Study information

Verified date February 2008
Source Maastricht University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The exact cause of the chronic lung disease sarcoidosis is still unknown. Consequently, a complete efficacious treatment is still not available. Earlier studies indicate an important key role for oxidative stress, i.e. an imbalance between the production of and the protection against ROS, in the etiology of sarcoidosis. Antioxidants, needed for protection against ROS, are indeed lower in sarcoidosis. Therefore, antioxidant therapy to strengthen the reduced antioxidant defense might be efficacious in sarcoidosis treatment. Since ROS are also capable of initiating and mediating inflammation, antioxidant therapy might also mitigate the elevated inflammation that occurs in sarcoidosis. The flavonoid quercetin possesses both anti-oxidative and anti-inflammatory capacities and might therefore serve as a good candidate for antioxidant therapy in sarcoidosis.

Therefore, the aim of the present study is to determine the effect of quercetin supplementation in sarcoidosis patients on markers of both oxidative stress and inflammation.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date January 2006
Est. primary completion date January 2006
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- clinical diagnosis of sarcoidosis with emphasize on pulmonary sarcoidosis

- no smoking

- no treatment

Exclusion Criteria:

- clinical diagnosis (and treatment) of other diseases

- symptoms of sarcoidosis in other organs besides the lung

- use of food supplements or vitamins

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
quercetin
1000 mg quercetin within 24 hours
Other:
placebo


Locations

Country Name City State
Netherlands Maastricht University Maastricht

Sponsors (2)

Lead Sponsor Collaborator
Maastricht University Medical Center ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary antioxidant status after 24 hours 24 hours
Primary inflammatory status after 24 hours 24 hours
Secondary plasma quercetin concentration after 24 hours 24 hours
Secondary plasma malondialdehyde (MDA) levels after 24 hours 24 hours
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