Status:

COMPLETED

BlueCQ Bioavailability

Lead Sponsor:

Heidelberg University

Conditions:

Methylene Blue

Chloroquine

Eligibility:

All Genders

18-50 years

Brief Summary

Bioavailability of methylene blue (MB) - comparison of an i.v. and two oral MB formulations - and influence of sustained release MB on chloroquine (CQ) concentrations in whole blood, plasma and urine....

Detailed Description

Maximum whole blood methylene blue (MB) concentrations after i.v. and oral administration may differ in the magnitude of 100:1. For achieving MB concentrations possibly effective against malaria when ...

Eligibility Criteria

Inclusion

  • Good state of health physically and mentally

Exclusion

  • Any regular drug treatment currently or past (within the last 2 months) except for oral contraceptives in females Treatment with a known inhibitor or inducer of drug metabolising enzymes or transport proteins within a period of less than 10 times the respective elimination half-life
  • Any acute or chronic illness, especially:
  • Glucose-6-phosphate dehydrogenase deficiency Allergic disposition or history of hypersensitivity reactions Smoking Alcohol or drug abuse

Key Trial Info

Start Date :

August 1 2004

Trial Type :

OBSERVATIONAL

End Date :

November 1 2004

Estimated Enrollment :

18 Patients enrolled

Trial Details

Trial ID

NCT00176072

Start Date

August 1 2004

End Date

November 1 2004

Last Update

September 15 2005

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