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WithdrawnNCT00988481

Topiramate Augmentation in Eating disorders Partial Responders

Medication studyAges 18–60United States
The study in practice

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Who could participate?

Listed age limits: 18 years to 60 years.

Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.

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What to know before participating

A point to clarify

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 dateSeptember 2009
Recruitment status
Withdrawn
Enrollment listed in the registry
0
Sponsor
Neuropsychiatric Research Institute, Fargo, North Dakota
Sponsor type
Research institute
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 18 Years to 60 Years
Official registry ID
NCT00988481
Official title
Show the full official title

Topiramate Augmentation in Bulimia Nervosa Partial Responders

Recruitment & locations

Withdrawn

Fargo

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Neuropsychiatric Research Institute, Fargo, North Dakota, a research institute.

Does this study involve medication?

Yes. The study involves medication, including Topiramate.

Who can participate?

Listed age limits: 18 years to 60 years.

Is this study still recruiting?

The registry lists this study as withdrawn.

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