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OpenTrials
Completed

NCT Number: NCT01816958

Neuromodulation to Facilitate the Effect of Ketamine

application of external neuromodulation along with ketamine infusion.

Completed

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Key information

Conditions

Depression Behavior Behavioral Symptoms Chemically-Induced Disorders Chronic Pain Mental Disorders Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms Substance Abuse Substance-Related Disorders

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The Neuroscience Center

Deerfield, Illinois, 60015, United States

About this study

apply TMS concurrent with ketamine infusion in order to increase the likliehood & strength of therapeutic benefit

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • chronically ill,
  • treatment-resistant

Exclusion criteria

  • active psychosis

Treatment and study plan

co-administration of TMS and infused ketamine

Other

co-administration of TMS and infused ketamine

Primary outcomes

  1. Global Assessment of Function in DSM-4R

    Time frame: up to 3 years

    treat in order to cause remission of disability

Sponsors and collaborators

Lead sponsor

The Neuroscience Center, LLC

Other

Registry information

Official study title

Treatment of Thalamocortical Dysrhythmia Using External Neuromodulation to Facilitate the Therapeutic Effect of Ketamine.

Acronym: TMS/ketamine

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Mar 22, 2013
Registry last updated
Mar 22, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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