Completed

Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression

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What is being tested

Reclaim™ DBS System

Device
Who is being recruted

Behavior+4

+ Mental Disorders

+ Behavioral Symptoms

Over 18 Years
+10 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-ControlledPhase 2
Interventional
Study Start: February 2009
See protocol details

Summary

Principal SponsorMedtronicNeuro
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2009

Actual date on which the first participant was enrolled.

Medtronic, Inc. sponsored an investigational study of the Reclaim™ Deep Brain Stimulation (DBS) System in people that have treatment-resistant depression. Depression is a mood disorder and a serious medical condition that affects millions of Americans. Depressive symptoms may include loss of interest in things typically enjoyed; decreased energy levels; difficulty concentrating or making decisions; restlessness; and feelings of pessimism, hopelessness, and worthlessness. Treatment-resistant depression is a chronic and severe form of depression characterized by failure to respond to traditional forms of treatment, such as antidepressant medications and electroconvulsive therapy. Treatment-resistant depression significantly impacts quality of life, productivity, and is a major contributor of disability world-wide. This randomized, double-blind, sham stimulation-controlled, multi-center, prospective, parallel design study used deep brain stimulation technology to test whether active bilateral stimulation can safely and effectively improve depressive symptoms in patients with treatment-resistant depression compared to sham stimulation. Participants meeting criteria for the study were implanted with the Reclaim DBS System. Participants in the active group, who received active stimulation, were compared to the control group, who received sham stimulation, during the 16-week blinded-treatment phase. All participants were monitored for changes in depressive symptoms. After the blinded-treatment phase, all participants received active stimulation. Candidates for the trial were adults who had major depressive disorder and had not responded to several treatments for depression. Participants in the study continued to receive their current antidepressant medications while participating in the trial.

Official TitleReclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression
NCT00837486
Principal SponsorMedtronicNeuro
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorMental DisordersBehavioral SymptomsDepressionDepressive DisorderMood DisordersDepressive Disorder, Treatment-Resistant

Criteria

6 inclusion criteria required to participate
Consent to participate in screening and study procedures by signing and dating the Informed Consent Form

Are diagnosed with major depressive disorder (MDD)

Have tried at least 4 different treatments, for example antidepressant medications, combinations of antidepressant medications, and/or electroconvulsive therapy (ECT)

Screening MADRS score ≥ 28

Show More Criteria

4 exclusion criteria prevent from participating
Females: Currently pregnant

Currently enrolled in or plan to enroll in any concurrent drug and/or device study that may confound the results of this study

Have a neurological condition that may jeopardize the safety or the conduct of the study

Have any medical conditions unsuitable for undergoing DBS surgery

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Active Comparator
Receive active stimulation with Reclaim™ DBS System

Group II

Sham
Receive sham stimulation with Reclaim™ DBS System

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 5 locations

Suspended

Massachusetts General Hospital

Charlestown, United StatesOpen Massachusetts General Hospital in Google Maps
Suspended

Cleveland Clinic Foundation

Cleveland, United States
Suspended

University of Pennsylvania

Philadelphia, United States
Suspended

University of Pittsburgh Medical Center

Pittsburgh, United States
Completed5 Study Centers