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TerminatedNCT01809340

The Effect of Minocycline on Relapse After Successful Intravenous Ketamine/Minocycline-induced Symptoms Response in Subjects With Depression

Medication studyAges 18–80Multiple countries
The study in practice

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Who could participate?

Listed age limits: 18 years to 80 years.

Listed locations
Duffel and 11 more locationsSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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What to know before participating

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This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateJune 2013
Recruitment status
Terminated
Enrollment listed in the registry
29
Sponsor
Janssen Research & Development, LLC
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
France, Belgium, Netherlands, ...
Age range
From 18 Years to 80 Years
Official registry ID
NCT01809340
Official title
Show the full official title

An Exploratory, Blinded, Randomized, Placebo-controlled Study in Subjects With Depressive Disorder to Investigate the Effect of Minocycline on Relapse After Successful Intravenous Ketamine/Minocycline-induced (Partial) Symptoms Response

Recruitment & locations

Terminated

Duffel, Belgium · Lede, Belgium · Leuven, Belgium

9 more locations
  • Besançon, France
  • Clermont-Ferrand, France
  • Nîmes, France
  • Leiden, Netherlands
  • Alicante, Spain
  • Barcelona, Spain
  • Coslada, Spain
  • Madrid, Spain
  • Zamora, Spain

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Janssen Research & Development, LLC.

Does this study involve medication?

Yes. The study involves medication, including Minocycline, Placebo and ketamine.

Who can participate?

Listed age limits: 18 years to 80 years.

Is this study still recruiting?

The registry lists this study as terminated.

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