Frequently Asked Questions

Signs may include:¹

• Feeling more thirsty than usual
• Urinating a lot
• Feeling very hungry
• Losing weight without trying
• Feeling irritable or having other mood changes
• Feeling tired and weak
• Having blurry vision

1. Source: https://www.breakthrought1d.org/t1d-basics/symptoms/

Hypoglycemia is the medical term for low blood sugar. In T1D, it means someone’s blood sugar has dropped below a safe range, causing symptoms like sudden shakiness, sweating, or confusion. There are research studies for type 1 diabetes focused specifically on nocturnal hypoglycemia (nighttime lows). These are dangerous overnight blood sugar drops that happen while someone sleeps and require immediate middle-of-the-night treatment.

While every study is different, currently enrolling local studies are looking for individuals between the ages of 18 and 75 who:

• Have lived with type 1 diabetes for at least 5 years.
• Are taking daily insulin injections or using an insulin pump.
• Experience low blood sugar, especially while sleeping, or have a glucose monitor that shows drops.
• Have an HbA1c level of 10.0% or lower.

Additional criteria apply. A trial doctor will determine final eligibility based on full medical criteria.

Yes. Type 1 and type 2 diabetes affect the body in different ways. Over time, individuals with type 1 diabetes often lose the natural hormone needed to naturally rescue the body from a blood sugar crash. Because this research focuses on preventing these specific types of nighttime drops, it is uniquely designed for individuals with type 1 diabetes.

The information gathered in clinical studies may help identify new treatment options in the future for people living with T1D. Study participants are often connected to specialists who understand their situation and can help answer questions from patients or their loved ones. 

Participants in research studies should expect to experience a professional clinical environment, be treated with compassion and respect, and have access to top quality study-related care during the clinical trial.

Most clinical trials will involve a screening visit to confirm that a potential participant is, in fact, a match for that trial’s criteria. Once verified, an Informed Consent Form, which clearly provides the details and purpose of the trial and what it involves, is reviewed with the participant for signature.

Participants can then expect to attend scheduled appointments at a trial clinician’s site. They may also receive a trial treatment (also called an investigational product) or potentially a control (also known as placebo, which contains no active treatment) and undergo additional  assessments  and follow-up monitoring. 

Throughout the trial, participants should experience a professional clinical environment and be treated with compassion and respect.

No, there is no cost to participate. For qualified participants who choose to be in this study, the study  drug will be provided at no cost. There will be no charge for any tests, examinations, nor visits done as part of this study. 

Participants may be reimbursed for travel costs and out of pocket expenses or these costs may be covered directly. They may also receive compensation for their time and effort.

There is no cost to participate in a clinical trial. Participants receive all study-related medical care and medications for the duration of the study at no cost. Likewise in many instances, participants may also receive reimbursement for their time and effort.

Participants may may receive compensation for their time and effort.

In any clinical study for a new treatment, there are potential risks, such as side effects of the study drug  or risks from the study activities. The study staff will explain these potential risks before participants decide whether to participate, and address any concerns.

No. Before a potential participant decides whether to take part in the study, the study staff will review the informed consent form with them and answer any questions. Once the consent form has been signed by the participant, the screening period of the study begins. During this period, the staff will review medical history and conduct any relevant assessments. Participants who meet all of the study criteria will be invited to participate

Yes. Participation in clinical trials is entirely voluntary. Even if a participant is already involved in a study, they may change their mind at any time, for any reason.

If you are interested in learning more, please contact us at any time. You may email us at help@clinicalenrollment.com.