RESEARCH / PARTICIPATIONBack to the library
← Find a study
Recruiting · registry status

Building a map of how the brain works

Researchers compile brain activity measurements into a shared map to help make better use of recordings collected in neurological care and research.

Learning by observing or collecting information · Study reference: NCT00575081

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

Open the official registry record ↗

Follow this study

Looking for volunteers

Start (reported date)
2006-08
Main measurements finished (planned)
2027-08
Study finished (planned)
2027-08

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Ages 6 years to 90 years · Does not accept healthy volunteers

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: all

Inclusion Criteria: * All patients who are recommended for Stereotactic Brain procedures * Any patient who has agreed to undergo a Stereotactic Brain procedure * Patients age under 6 -90 years old Exclusion Criteria: * Patients who fail recommendation for Stereotactic Brain procedures * Patients not consented for Stereotactic Brain procedures * Patients outside the age range of 6 -90 years old * Patients or legal guardians not able to provide informed consent
Full study name & original research details

Official study title

Physiological Brain Atlas Development

Original description

The NIH grant has funded the development of a physiological brain atlas registry that will allow us to significantly improve the data collectioin and use of physiological data into a normalized brain volume. This initially was used to improve DBS implants for Parkinson's Disease, Dystonia, Essential Tremor, and OCD, but now includes data acquired during all stereotactic brain procedures.

Further description from the registry

Purpose: 1. To create a brain atlas that will allow physiological and clinical information to be assigned to anatomical locations in MRI space, utilizing non-rigid MRI normalization algorithms. These data will specifically be acquired from the population of patients undergoing stereotactic brain procedures. 2. To collate and analyze the brain data placed in the atlas in a statistical manner that allows doctors to understand and treat brain disease more precisely and based on population data. For example, this would allow surgeons to predict optimal targeting locations for DBS implants, neurologists to program implants based on multiple physiological variables, including pre-operative severity of disease, intraoperative neurophysiological observations, and post-operative responses to previous therapies in a larger population of subjects. 3. To allow precise relationships to be visualized in one anonymized MRI volume, which can lead to new findings across larger populations of subjects in the field of brain science. 4. To locate all the data in a HIPAA compliant, anonymized location that clinicians and researchers can access securely without compromising personal healthcare information (PHI). Protocol: 1. Patients who have consented to undergo or have undergone a stereotactic brain procedure for any reason will be asked to participate in this study. 2. Permission from the patient will be sought to allow the entry of all related data to be entered into the atlas database. Specifically, this includes any and all related pre-operative, intra-operative, and post-operative clinical, radiographic, and psychologic testing done for the purposes of the surgery. 3. The data must be entered in a confidential fashion and secured within a section of the database that can be accessed only by persons authorized to view patient healthcare information (PHI). Persons authorized to enter and view individual PHI must have taken and passed the CITI certification and presented documentation of this credential to the IRB study investigator (Dr. Konrad) or his Clinical Trials Specialist (Melba Isom). 4. Access to individual patient data within the database can be done through a secure login linked to the person's qualifications to access PHI. The list of authorized persons (such as treating physicians and members of the surgical team) will be determined by Dr. Konrad and updated at least on an annual basis within the database by Dr. Dawant. Dr. Dawant will be responsible to ensure that PHI is physically and virtually secure within the atlas database. 5. Once in the database, patient identifiers will be codified and not accessible for any queries outside of those certified in step 3. Non-patient specific information can be analyzed, sorted or queried in response to specific statistical questions by any investigator of the research team or authorized person, as designated by the database developer (Dr. Dawant) or his designee. 6. Data contained within the atlas will be analyzed and regularly reported to members of the Atlas research team regarding accurate display and representation of the data. 7. Clinical and physiological data will continue to be entered for every subject who consents to participate in this study for the duration of their care. 8. If subjects no longer wish to have their data tracked within the atlas, they can call the study coordinator (Melba Isom) and have their name removed from any further data collection from the time of notification forward. All previously collected data will still be accessible and not expunged from the database. 9. We plan to recruit 5,000 patients from Vanderbilt and participating sites.

Conditions reported: Parkinson's Disease; Obsessive Compulsive Disorder; Dystonia; Essential Tremor; Epilepsy

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Observational
Interventions
Stereotactic brain procedures
Phases
Not reported
Sponsor
Vanderbilt University Medical Center
Start date reported by registry
2006-08 (Not reported)

Registry updated: 2026-08-26 · Status last verified by the registry submitter: 2026-08

Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Dario J Englot, MD, Ph.D. · 615-322-7417 · dario.englot@vumc.org

Wuraola a Adesinasi · wuraola.a.adesinasi@vumc.org

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

Vanderbilt Univeristy

Nashville, Tennessee, United States

Recruiting

Dario J Englot, MD, Ph.D. · 615-322-7417 · dario.englot@vumc.org

Wuraola T Adesinasi@vumc.org · wuraola.a.adesinasi@vumc.org

Benoit Dawant, Ph.D.

Hong Yu, MD

Changqing Kao, MD, Ph.D.

Dario Englot, MD, PhD

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.