Teen Bone Mineral Density Study
You can make a difference for women’s health.
Consider joining the Lotus study, a bone mineral density study for birth control users.
The Lotus study will explore whether two hormonal birth control pills affect women’s bone mineral density. The pills are a tablet called LF111 (marketed in the United States under the commercial name SLYND) and its chewable version, called Drospirenone (DRSP) chewable tablets.
You may be able to join if you are 14-17 years old and are willing to use the same birth control for 1 year. You will be able to choose between a variety of birth control options, including sexual abstinence.
Other study requirements apply.
Study participants receive at no cost:
- The opportunity to use LF111 tablets or DRSP chewable tablets for a full year.
- Blood and urine tests, physical exams, and at least 3 consultations with the study doctor.
- At least 2 bone scans (non-invasive and painless) that will give you information on your bone health and body mass composition.
- Education about hormonal birth control.
- The opportunity to help other women learn about hormonal birth control.
A clinical trial is a carefully designed research study involving human volunteers to investigate the safety and effectiveness of a new drug or treatment. Clinical trials are essential for evaluating the benefits and risks of medical interventions, ultimately informing healthcare decisions and regulatory approvals.
As a clinical trial or observational study participant, your responsibilities and what you will be required to do can vary depending on the study, its objectives, and the phase of the trial.
Some common activities and responsibilities you may encounter as a participant include: diagnostic tests, treatments, procedures, doctor visits, dietary changes, exercise and/or other lifestyle changes. Observational studies often involve minimal effort, such as completing questionnaires, sharing test results, maintaining a diet or exercise log.
Joining a clinical trial can provide access to cutting-edge treatments, close medical monitoring, and an opportunity to contribute to medical knowledge. Participants may experience improved health outcomes and specialized care while potentially receiving compensation for volunteering.
Clinical trials are designed with a strong emphasis on the safety of participants, and multiple safeguards are in place to minimize risks, including careful study design, oversight by institutional review boards and routine monitoring of study data by independent experts. Researchers must inform participants of the risks, benefits and/or side effects they discover.
Yes, you can drop out of a clinical trial study at any time, and you have the right to do so without facing any penalties or consequences. This is often referred to as "withdrawal of consent."
Voluntary participation is a fundamental principle of clinical research. You are not obligated to continue in a trial if you no longer wish to do so.
Determining your eligibility to participate in a clinical trial involves a thorough evaluation of specific eligibility criteria set forth by the study's researchers and sponsors. The criteria help define the patient population being studied and are designed to protect the safety of participants in the trial.
Providing accurate information about your medical history and health status is crucial for your safety and the integrity of the research. If you are not eligible for one trial, you may still be eligible for other trials in the future, so it's worth exploring your options if you are interested in participating in clinical research.