Explore Our Upcoming Studies
Our available studies are listed below and are updated regularly. To view details about a study, please click on the specific study box below.
To pre-register for a study, simple select the Register Now button. If you have questions, please feel free to reach out to us at 602-346-4747.
- $680*18+ years of age
- Enrolling Now
- TBD40-80 years of age
- 185018 - 55 years of age
- Healthy Volunteer
- Currently Enrolling
IPF or Idiopathic Pulmonary...
- Compensation Avail40 + years of age
- Pulmonary Fibrosis
- Currently Enrolling
- $1490.0018-50 years of age
PACT Is A World Leader In Pulmonary Research
Under the direction of Dr. Mark Gotfried, a Certified Principal Investigator, PACT investigators have conducted over 500 studies with at least 100 sponsors and more than 15 CROs in all phases of clinical research. Experience such as this, combined with the excellence of our full-time study coordinators, a full-time pulmonary function technician, and a regulatory document specialist enable us to provide sponsors with a research staff that is able to anticipate enrollment challenges and address the situation before precious time is wasted, helping to keep sponsors’ budgets and timelines on track.
PACT has significant experience and expertise in all aspects of pulmonary diseases and sleep disorders. In addition PACT has many years in research experience in the field of pharmacokinetics and pharmacodynamics (PK/PD) with multiple studies on lung PK/PD published in peer review literature.
Our research is supported by 18 providers with sub investigators having significant research experience. Recent research has been done with subjects who have Asthma, COPD, Pulmonary Fibrosis, Pulmonary Hypertension, Bronchiectasis, Insomnia, Sleep Apnea, Narcolepsy and Idiopathic Hypersomnia.
We have an extensive database, which allows us to successfully enroll patients into our research studies, and our familiarity with these areas helps us avoid potential pitfalls that others might have, as evidenced by our low screen failure rates.
Over 500 studies completed
Screening and Enrollment Goals Met
Rapid Study Startup
Low Screen Fail Rates
Frequently Asked Questions
WHAT ARE THE BENEFITS AND RISK OF CLINICAL TRIALS?
The benefits vary depending on the study you are participating in. Participants may get a new treatment for a disease that is not currently available to everyone else. You are given the opportunity to play a more active role in your own health care. You also are helping play a role in the effort to provide new medications and information that might benefit other people who have the disease. You will receive no cost medical care during your study. We understand that your time is valuable therefore most of our studies do compensate for time and travel. There are risks of side effects that might occur during a study. You would be informed of those risks. Studies are designed to minimize risks as much as possible and you would be closely monitored throughout your participation for your safety.
DO I NEED A MEDICAL CONDITION TO PARTICIPATE?
That will depend on the study you are interested in. Our office typically participates in two different types of studies.
Diagnosis Specific studies do require a medical diagnosis, such as Asthma, COPD, and Pulmonary Fibrosis. In the list of current studies available it will include what specific diagnosis you should have prior to participating.
Healthy Volunteer Studies are looking for healthy individuals that have not been diagnosed with any medical conditions and are not on any prescription medications. These studies are usually performed to get an idea how a medication is distributed throughout the body and to help get a better idea of the possible side effects from using the study medication.
WHAT CAN I EXPECT DURING A STUDY?
Step 1: The first step is to contact our office. You can call our office at 602-346-4747, or fill out the Contact Me form and we can get in touch with you as well.
Step 2: It is important to screen your medical history and explain the study to you over the phone. It generally takes about 10 minutes to complete a phone screen so we make sure you will fit the guidelines set by the protocol. If you don’t meet criteria the first time, with your permission we can add you to our database for future studies you may qualify for.
Step 3: Once you’ve been prescreened and determined a potential good fit for the study we will schedule an office visit to review the study as part of an informed consent process and go over the informed consent after you have had as much time as you need to review the informed consent form. You will spend time with the coordinator and Principal Investigator making sure you understand and feel comfortable participating in the study.
Step 4: If you agree to participate and meet all the criteria and sign all the Informed Consent documents assessments called for by the study will be begun to make sure that you are eligible.
Step 5: Each study has different study schedules and your coordinator will go over that in detail with you. Generally all studies require blood draws, EKG’s and office visits. Some studies will require additional items like completing a daily diary, or sleep studies. Each protocol has different requirements. A complete study schedule will be given to you during your first office visit.
WHAT DO I NEED TO BRING TO MY FIRST APPOINTMENT?
We understand it can be difficult to remember every diagnosis or surgery throughout your life. Before you come in to our office we ask that patients make a list of any previous diagnosis’s, surgeries and a list of current medications with doses and bring that list with you. Also we will request medical records from your physician so it is helpful if you can bring their phone number/fax number.
Ready to see if you qualify for one of our Pulmonary, Sleep and Research Studies through PACT?
About Our Research Center
At Pact we are proud to continue to provide excellent service in our legacy areas of pulmonary trials, sleep disorders and pharmacokinetic studies. Our two state-of-the-art facilities provide our participants with a cardio pulmonary exercise (CPX) unit, a pulmonary function lab, sleep lab with bed availability prioritized for research subjects, along with beds in our office for overnight visits, onsite x-ray equipment, ECG machines, IV Pumps, and more.
We are always focusing on how we can be that site at the top of the list when sponsors are recruiting investigative sites. We assess our resources, staff, and equipment and research space regularly to make sure we are doing everything possible to make PACT a “go to” site for sponsors and CRO’s. We are pleased to have many sponsors return to our research site time and time again to get the same quality that they have come to know and expect from our site.
Sponsor A Trial With Pulmonary Associates
We appreciate the opportunities we have had to partner with the many sponsors and CROs that we have worked with to date, and welcome discussions regarding our capabilities and experience as they relate to potential new studies. Our mission is to conduct clinical trials successfully with exacting standards in order to build longstanding relationships with our customers. We look forward to hearing from you.
About Our Doctors
Mark Gotfried, MD
Medical Director/Principal Investigator
Dr. Gotfried received his degree in medicine with honors from the University of Illinois. He completed his internship and residency both at Michael Reese Hospital in Chicago followed by his pulmonary fellowship at the University of Arizona in Tucson. Dr. Gotfried joined Pulmonary Associates in 1983 and is board certified in Internal Medicine, Pulmonary Disease and Sleep Disorders Medicine. Dr. Gotfried has over 30 years of clinical research experience in a variety of therapeutic areas. In addition to his practice and research work, Dr. Gotfried is a Clinical Professor of Medicine at the University of Arizona and an Adjunct Professor of Pharmacy Practice at the University of Illinois. Dr. Gotfried is a Certified Principal Investigator. He has served as a consultant in numerous advisory boards regarding clinical trials.
David Baratz, MD
Dr. Baratz received his MD from the University of Arizona College of Medicine. He is board-certified in Internal Medicine, Pulmonary Medicine and Sleep Medicine. He has been conducting clinical research for over 15 years and his research specialties include: sleep disorders, COPD, Asthma, and Pulmonary Arterial Hypertension.
J. Burr Ross, MD
Dr. Ross attended the University of Nebraska, where he received his MD degree. He is board-certified in both Internal Medicine and Pulmonary Disease. His 15 years of research experience includes extensive work in invasive Bronchoscopic technique for emphysema and cancer diagnosis.
Stephen R. Anthony, MD
Dr. Anthony received his MD from Medical College of Wisconsin. He has been an integral part of clinical research and offers more than 15 years’ experience conducting studies. He is board certified in Pulmonary and Sleep medicine.