treat in order to cause remission of disability
Neuromodulation to Facilitate the Effect of Ketamine
Brief Summary
application of external neuromodulation along with ketamine infusion.
Condition or Disease
- Depression
- Chronic Pain
- Substance Abuse
Phase
Study Design
Study type: | OBSERVATIONAL |
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Status: | Completed |
Study results: | No Results Available |
Age: | 18 Years and older (Adult, Older Adult) |
Enrollment: | 35 (ACTUAL) |
Funded by: | Other |
Time Perspective: | Retrospective |
Observational Model: | Case-Control |
Masking |
Clinical Trial Dates
Start date: | Jan 01, 2011 | |
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Primary Completion: | Nov 01, 2012 | ACTUAL |
Completion Date: | Nov 01, 2012 | ACTUAL |
Study First Posted: | Mar 22, 2013 | ESTIMATED |
Results First Posted: | Aug 31, 2020 | |
Last Updated: | Mar 20, 2013 |
Sponsors / Collaborators
Location
apply TMS concurrent with ketamine infusion in order to increase the likliehood \& strength of therapeutic benefit
Participant Groups
-
co-administration of TMS and infused ketamine for patients with chronic pain of psyche and/or soma
Eligibility Criteria
Sex: | All |
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Minimum Age: | 18 |
Age Groups: | Adult / Older Adult |
Healthy Volunteers: | Yes |
Inclusion Criteria:
* chronically ill,
* treatment-resistant
Exclusion Criteria:
* active psychosis
* chronically ill,
* treatment-resistant
Exclusion Criteria:
* active psychosis
Primary Outcomes
More Details
NCT Number: | NCT01816958 |
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Acronym: | TMS/ketamine |
Other IDs: | 12_1293 |
Study URL: | https://clinicaltrials.gov/study/NCT01816958 |
Last updated: Sep 29, 2023