Volunteers
There are certain requirements which must be met to be eligible to participate in a clinical study. These requirements are based on such factors as age, gender, the
type and stage of a disease, previous and current treatments, and other medical conditions. Medical insurance is not required to participate in clinical studies or to receive
study-related medical care and services.
Study Participation
If you are eligible and decide to participate, an informed consent document will be presented to you. This document includes information about the clinical study and what
you can expect as a participant, as well as potential benefits and possible risks associated with the research. You should take your time and read carefully through the
informed consent document. When you are satisfied that all of your questions have been answered, you will be asked to sign the document.
At SDS Clinical Trials, we are committed to protecting the rights and welfare of people who volunteer for research.
SDS Clinical Trials
All clinical trials have guidelines about who can participate. Before joining a clinical trial, a volunteer must qualify for the study. The factors that allow volunteers to participate in a clinical trial are called "inclusion criteria" and the factors that disallow volunteers from participating are called "exclusion criteria." These criteria can include age, gender, previous medical history, and other medical conditions.
Some research studies seek participants with specific illnesses or conditions to be studied in a clinical trial, while others require healthy participants. It is important to note that inclusion and exclusion criteria are used to identify appropriate participants, promote participants' safety, and ensure that researchers learn the information
they need.
Contact Us
If you qualify to participate in a clinical research study, you will be asked to make several visits to our study site. You will receive all study-related medications and procedures at no cost and you may be compensated for your time and travel. To find out if you qualify for one of our clinical research studies, please
call us or type in your name and phone number in the space below and we´ll call you. All calls are strictly confidential.Thank you for your interest in our clinical research studies.
Se Habla Espanol
1535 E. 17th St, Suite 101, Santa Ana, CA 92705
(714) 834-1565
Fax (714) 834-1551
Fields of Study
Adolescents/PediatricsAllergy/Immunology Anxiety and Depression Arthritis/Rheumatoid Arthritis
Cardiology
Cold and Flu Treatment
Dermatology
Diabetes/Endocrinology
Diabetic Painful Neuropathy
GERD/Heartburn
Hypercholesterolemia/High Cholesterol
Hypertension/High Blood Pressure
Insomnia/Sleep Disorders
Irritable Bowel Syndrome
Menopause/Women's Health
Migraine/Chronic Headache
Neurology/CNS
Obesity
Osteoporosis/Osteopenia
Pain Management
Respiratory
Restless Leg Syndrome
Urology Vaccines
Our Facilities
Our services include:
Full Time Dedicated Phase II - IV Clinical Trial Abilities
Full Service Sleep Lab, Certified
Real Time Reporting for Sponsors
Private On-Site Full Service Monitoring Stations/Rooms
Healthy Population Trials
Pediatric, Adult and Geriatric Populations
100,000+ patient database
ECG
PH Monitoring
Pharmacokinetics
Pharmacogenetics
Drug to Drug Interactions
Dietician Support
Data Management
Quality Assurance
Protocol Review and Development
Equipment
Electronic Capture ECG Machines
Manual & Electronic Capture Vital Sign Machines
-70° Freezer
-20° Freezer
Refrigerated Drug Storage
Refrigerated Centrifuges
Centrifuges
Refrigerated Specimen and Blood Storage
Secure Drug Storage
Secure Computer Access
Dedicated, Digital and Analog Telephone Lines
At SDS Clinical Trials, our specialty is providing sponsors and CROs with rapid study enrollment, high subject retention, meticulous data and meeting critical timelines. By utilizing a central IRB combined with our 100,000+ patient database, our energetic and experienced, bi-lingual staff ensures SDS Clinical Trials will meet and exceed goals efficiently. SDS Clinical Trials' commitment to clinical research ensures patient safety, quality, and efficiency. The diversity among our experienced team provides great benefit to the
research community. With more than 20 years experience, our Principal and Sub-Investigators are Board Certified in a wide range of therapeutic areas and are dedicated to treating study patients with the utmost dignity and compassionate care. Our highly motivated research team has outstanding ethics and values putting patient safety first. Our experienced staff is knowledgeable and strictly follows the FDA regulations, ICH/GCP guidelines, IRB standards, HIPAA and Sponsor requirements. Please view Our Code of Ethics.