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Clinical trial

A Randomized, Two-way Crossover Study to Compare the Bioavailability of 300 mg Trazodone Hydrochloride Extended-release Caplets (Containing Contramid®) (Administered as a Single Dose) and 100 mg Trazodone Hydrochloride Immediate-release Tablets (Administered Three Times Daily) Under Fasting Conditions

NCT01121900 is registered in ClinicalTrials.gov with Labopharm Inc. as lead sponsor.

NCT NCT01121900
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Two-way Crossover Study to Compare the Bioavailability of 300 mg Trazodone Hydrochloride Extended-release Caplets (Containing Contramid®) (Administered as a Single Dose) and 100 mg Trazodone Hydrochloride Immediate-release Tablets (Administered Three Times Daily) Under Fasting Conditions
Lead sponsor
Labopharm Inc.
Phase
Phase 1
Overall status
Completed
Start date
June 30, 2008
Completion date
July 31, 2008
Enrollment
26 (actual)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

healthy