Normal Volunteers Clinical Trial
Official title:
Tissue Procurement for Biomedical Research
The need to obtain human tissue for methods development and disease correlation is frequent in Biomedical Research Center laboratories. This protocol is designed to create the opportunity to obtain such tissue samples including: blood, urine, saliva, sweat, feces, hair and nail clippings, nasal scraping, muscle, fat, skin and taste buds. It may also include samples taken during a surgical procedure, including: fluid from around the spinal column, heart, lungs and abdomen; fat, muscle, connective tissue and organs (liver, bladder, heart, kidney and skin). Information derived from such studies is for research purposes only and is not provided to the participants or their health care provider. Samples will be coded (no names) and identifying information linking the participant to the sample will be maintained in a secure location by the P.I. and Study Coordinator. Participants will be 18 years or older and have been identified by the investigator and/or physician to have a condition of interest for exploratory studies related to the participant s illness or other feature that offers the possibility of creating information that leads to scientifically useful and important studies. Participants could also be healthy volunteers, willing to provide their samples. These samples could be requested by an investigator to be used as age, gender, race and/or ethnicity-matched controls or to calibrate or compare and contrast across lab equipment. Participants will be excluded if obtaining the sample would be over and above usual clinical care, would result in excessive blood loss, or the individual is unable to provide informed consent. The expected outcome is to provide investigators with the opportunity to obtain tissues of interest for laboratory evaluation....
The need to obtain human tissue for methods development and disease correlation is frequent in Biomedical Research Center laboratories. This protocol is designed to create the opportunity to obtain such tissue samples including: blood, urine, saliva, sweat, feces, hair and nail clippings, nasal scraping, muscle, fat, skin and taste buds. It may also include samples taken during a surgical procedure, including: fluid from around the spinal column, heart, lungs and abdomen; fat, muscle, connective tissue and organs (liver, bladder, heart, kidney and skin). Information derived from such studies is for research purposes only and is not provided to the participants or their health care provider. Samples will be coded (no names) and identifying information linking the participant to the sample will be maintained in a secure location by the P.I. and Study Coordinator. Participants will be 18 years or older and have been identified by the investigator and/or physician to have a condition of interest for exploratory studies related to the participant s illness or other feature that offers the possibility of creating information that leads to scientifically useful and important studies. Participants could also be healthy volunteers, willing to provide their samples. These samples could be requested by an investigator to be used as age, gender, race and/or ethnicity-matched controls or to calibrate or compare and contrast across lab equipment. Participants will be excluded if obtaining the sample, would result in excessive blood loss, or the individual is unable to provide informed consent. The expected outcome is to provide investigators with the opportunity to obtain tissues of interest for laboratory evaluation. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02922933 -
A Study to Examine the Effect of Omeprazole, Famotidine, and an Acidic Beverage on the Pharmacokinetics of Entinostat in Healthy Adult Subjects
|
Phase 1 | |
Completed |
NCT02922946 -
Study to Determine the Effect of the Timing of a Meal on the Pharmacokinetics of Entinostat
|
Phase 1 | |
Completed |
NCT01250197 -
Formulation Comparison in Normal Volunteers
|
Phase 1 | |
Completed |
NCT02051517 -
Vitreous Chemistry Analysis
|
N/A | |
Completed |
NCT01185418 -
Evaluation of Negative Symptoms and Cognitive Function After Administration of Antipsychotics in Healthy Volunteer
|
N/A | |
Completed |
NCT02828813 -
Neural Mechanisms of Motor and Cognitive Networks
|
||
Completed |
NCT02146391 -
Study to Evaluate the Effect of Food Upon the Pharmacokinetics of Androxal
|
Phase 1 | |
Terminated |
NCT00465842 -
Protein Biomarker in Hepatocellular Carcinoma
|
||
Recruiting |
NCT02471352 -
Studies of Dermatologic Diseases Biospecimen Acquisition Protocol
|
||
Terminated |
NCT01752231 -
Optimization of Novel DCE-MRI Imaging Sequences for Cancer Therapy Monitoring
|
N/A | |
Completed |
NCT02517307 -
Fatty Acid Oxidation Defects and Insulin Sensitivity
|
N/A | |
Completed |
NCT01366352 -
Pharmacokinetics and Bioavailability Comparison of Two Different Formulations of MNTX Tablets
|
Phase 1 | |
Not yet recruiting |
NCT01487486 -
Proteomics & Glyco-Proteomic Analysis of Follicular Fluid
|
N/A | |
Completed |
NCT03993587 -
The Effect of Head and Shoulder Positioning on the Cross-sectional Area of the Subclavian Vein in Obese Adults
|
||
Completed |
NCT02860351 -
The Effect of Head Positioning on the Cross-sectional Area of the Subclavian Vein.
|
N/A | |
Completed |
NCT02113943 -
Double Blind Randomized, Monocentric, Cross-over, Placebo-controlled Study to Evaluate the Effect of Citalopram on Motivation
|
Phase 2 |