Long-term Follow-up in Patients With Deep Brain Stimulation (DBS) for Obsessive Compulsive Disorder (OCD).
1 other identifier
observational
30
1 country
1
Brief Summary
For this human research, 17 treatment-refractory OCD patients who already received DBS implants for treatment refractory OCD between June 1998 and October 2007 will be included. New patients that complete the protocol on "refining the target for DBS in OCD" will be included in this follow-up study as well. They will be psychiatrically evaluated on regular bases: at least twice yearly in the years two to five after surgery, at least once a year for the years thereafter. The duration of this protocol is indefinite, but spans at least 10 years. The main aim of this study is to investigate the long-term effect of DBS in OCD patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2008
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2008
CompletedFirst Submitted
Initial submission to the registry
June 12, 2013
CompletedFirst Posted
Study publicly available on registry
June 17, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 5, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
February 5, 2015
CompletedJuly 10, 2024
July 1, 2024
7 years
June 12, 2013
July 9, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Yale-Brown Obsessive Compulsive Scale (Y-BOCS)
up to 10 years
Study Arms (1)
DBS for OCD
Interventions
Eligibility Criteria
Patients that have received DBS for OCD will be included in this study.
You may qualify if:
- Patients who have received DBS implantation for the treatment of OCD
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UZ Leuven
Leuven, Vlaams-Brabant, 3000, Belgium
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 12, 2013
First Posted
June 17, 2013
Study Start
February 1, 2008
Primary Completion
February 5, 2015
Study Completion
February 5, 2015
Last Updated
July 10, 2024
Record last verified: 2024-07