Neurological Surgery & Affiliated Services De-Identified Clinical Outcomes Database

NCT00593411 | Completed DMC

• 2 other identifiers: 2005-4323MDA4323
• Study Type: observational
• Target: 732
• Locations: 1 country
• Sites: 1

Brief Summary

The collection of data from the myriad of services described is significantly impacted by NIH guidelines defining medical research involving humans as well as the recent implementation of HIPAA constraints which further complicate the conduct of retrospective clinical outcomes research. Simple case reports or case series analysis now involve IRB participation as well as voluminous documentation. The solution to this dilemma lies in developing and promoting secure, confidential prospective clinical databases for storing clinical data for subsequent retrospective de-identified inquiry. These databases function in a way analogous to "tissue banks" for subsequent basic science research. Patients consent to prospective entry of their clinical information into the database so long as they continue to be a patient with the Department of Neurological Surgery or the Departments or Divisions in association with the affiliated programs briefly described above. The consent is obtained during the patient's first inpatient or outpatient encounter in parallel with the HIPAA consent. It can be withdrawn by request of the patient at any time, but it does not expire unless the patient withdraws it, or the patient severs their patient care relationship with UCI Neurosurgery or the affiliated programs. The database is stored on a separate secure server maintained and backed up by the UCIMC Information Technology Department. Access to the database is restricted at multiple levels, with the majority of personnel allowed only limited access for data entry purposes. Only the database programmer/coordinator, the Department Administrator and the Chairman of the Department will have unrestricted access to the database. Authority for permission for levels of security clearance and access to the database, for other individuals, will be vested in the Chairman of the Department of Neurological Surgery. A separate IRB proposal will be formulated for individual study related to the acquisition of data from the de-identified database. Since these future studies will be performed on data sets derived from the previously consented subjects of this IRB-approved project, the requirement for additional consent forms are not anticipated. As a result IRB research proposals utilizing the database can be expedited. Once the specific study is approved, the investigator(s) are provided with the clinical information from the database in the form of a de-identified data set.

Conditions

Central Nervous System Disorder; Spine Disease; Peripheral Nerve Disorder

Keywords

MD Analyze; Central Nervous System; Spine Disease; Peripheral Nerve

Eligibility Criteria

• Age: 7 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

All UCI patients with central nervous disorder, spinal disease or peripheral nerve disorder

You may qualify if:

• Patient of one of the investigators mentioned in the IRB Protocol Narrative
• Ability to give informed consent to have health care info collected, stored, analyzed
• Ability to sign HIPAA form

You may not qualify if:

• Nonpatient of one of the investigators in the study
• Minors under the age of 7
• Patients without the ability or capacity to give informed consent

Sponsors & Collaborators

• University of California, Irvine: lead

Study Sites (1)

University of California, Irvine - Medical Center

Orange, California, 92686, United States

Location

MeSH Terms

Conditions

Central Nervous System Diseases; Spinal Diseases; Neuritis

Condition Hierarchy (Ancestors)

Nervous System Diseases; Bone Diseases; Musculoskeletal Diseases; Peripheral Nervous System Diseases; Neuromuscular Diseases

Study Officials

• Mark Linksey, MD

  University of California, Irvine

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 3, 2008
• First Posted: January 15, 2008
• Study Start: August 4, 2005
• Primary Completion: June 9, 2012
• Study Completion: June 9, 2012
• Last Updated: March 29, 2021

Record last verified: 2021-03

Locations

US (1)