Systems And Methods Of Conducting Clinical Research

• US 20070239782A1
• Filed: 11/24/2006
• Published: 10/11/2007
• Est. Priority Date: 11/23/2005
• Status: Active Grant

• Current Assignee: Qualcomm, Inc.
• Original Assignee: Ultra-Scan Corporation (Qualcomm, Inc.)
• Inventors: Schneider, John
• Granted Patent: US 7,937,423 B2
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: G06Q 10/00 Administration; Management
• CPC Class Codes: G06Q 10/10 Office automation; Time management
• CPC Class Codes: G06Q 50/00 Information and communication technology [ICT] specially adapted for implementation of business processes of specific business sectors, e.g. utilities or tourism healthcare informatics G16H
• CPC Class Codes: G16H 10/20 for electronic clinical trials or questionnaires
• CPC Class Codes: G16H 10/40 for data related to laboratory analysis, e.g. patient specimen analysis
• CPC Class Codes: G16H 10/60 for patient-specific data, e.g. for electronic patient records
• CPC Class Codes: G16H 70/00 ICT specially adapted for the handling or processing of medical references
• CPC Class Codes: Y10S 707/966 Distributed

Abstract

Information management systems for clinical research, and related methods, are disclosed. The management system may have a database of biometric sample information. At least some of the pieces of sample information in the database may have been received from a test-subject in a first clinical research effort, and each piece of sample information may have a related pointer stored in the database. Each pointer may identify the location of clinical research information obtained during the first clinical research effort.

Claims

1. A clinical research management system, comprising:

a database of biometric sample information, at least some of the pieces of sample information having been received from a test-subject in a first clinical research effort, and each piece of sample information having a related pointer to clinical research information obtained during the first clinical research effort;

a check-in facility at a clinical research facility that is conducting a second clinical research effort, the check-in facility having a biometric reader;

a communication channel;

a microprocessor, programmed to;

(a) receive from the communication channel, information corresponding to a biometric specimen received at the check-in facility, (b) compare the biometric specimen to the biometric sample information (c) determine whether the specimen matches at least one piece of the sample information to identify a matching piece of sample information, (d) identify the pointer related to the matching piece of sample information, (e) use the pointer to obtain the corresponding clinical research information obtained during the first clinical research effort, (f) provide the obtained corresponding clinical research information to the clinical research facility conducting the second clinical research effort.

2. The management system of claim 1, further comprising a second database, the second database having stored therein the clinical research information obtained from the test-subject during the first clinical research effort.

3. A clinical research management network, comprising:

a first database of biometric sample information, at least some of the pieces of sample information having been received from a test-subject in a first clinical research effort, and each of those pieces of sample information having a related pointer to clinical research information obtained during the first clinical research effort;

a plurality of check-in facilities, each check-in facility being located at a clinical research facility that is conducting clinical research that is not related to the first clinical research effort, and each check-in facility has a biometric reader;

a microprocessor in communication with the check-in-facilities and the first database, and programmed to;

(a) receive a biometric specimen received at the biometric reader of one of the check-in facilities, (b) compare the biometric specimen to the biometric sample information (c) determine whether the specimen matches at least one piece of the sample information to identify a matching piece of sample information, (d) identify the pointer related to the matching piece of sample information, (e) use the identified pointer to obtain the corresponding clinical research information obtained during the first clinical research effort, (f) provide the obtained corresponding clinical research information to at least one of the clinical research facilities conducting clinical research that is not related to the first clinical research effort.

4. The management network of claim 3, further comprising a plurality of second databases, each of the second databases having stored therein clinical research information pointed to by the pointers of the first database, and wherein at least one of the second databases has the clinical research information obtained during the first clinical research effort.

5. A method of managing clinical research, comprising:

providing a database having biometric sample information, each piece of sample information having been received from a test-subject in a first clinical research effort, and each piece of sample information having a related pointer to clinical research information during the first clinical research effort;

providing a prospective test-subject at a clinical research facility conducting a second clinical research effort;

obtaining a biometric specimen from the prospective test-subject;

comparing the biometric specimen to the biometric sample information;

determining whether the specimen matches at least one piece of the sample information;

if the specimen matches at least one piece of sample information, then using the related pointer to obtain the corresponding clinical research information obtained during the first clinical research effort;

providing the obtained clinical research information to the clinical research facility conducting the second clinical research effort;

determining whether the obtained clinical research information indicates a problem with the prospective test-subject participating in the second clinical research effort, to provide a determination;

acting on the determination by allowing the prospective test-subject to participate in the second clinical research effort if the determination does not indicate a problem, or preventing the prospective test-subject from participating in the second clinical research effort if the determination indicates a problem.

6. The method of claim 5, wherein the pointer points to a database other than the database having biometric sample information.