Your Chance to Contribute to Medical Advancements

Frequently Asked Questions

• Who can participate in a study?

  The criteria vary depending on the study. Some require participants with specific medical conditions, while others might seek healthy volunteers.

• Will I be compensated for my time?

  Many studies offer compensation for time and travel. The specifics will be discussed during the screening process.

• What happens if I experience side effects during the trial?

  Monitoring participant well-being is a continuous process throughout the trial. If you experience any side effects, it’s vital to report them immediately to the study team. Our medical professionals are trained to address and manage any adverse reactions promptly. Your health and safety are always our main concern, and necessary adjustments or interventions will be made to ensure your well-being.

• How are the safety and rights of clinical trial participants protected?

  At Momentum, participant safety and rights are our utmost priority. All clinical trials are guided by strict ethical principles and overseen by independent ethics committees. Prior to starting, participants are provided with an informed consent form detailing the study, its potential risks, and benefits. Participants have the right to withdraw at any point, and all personal information is handled with the utmost confidentiality.

• How long will the clinical trial last, and how often will I need to visit the trial site?

  The duration of a clinical trial and the frequency of visits depend on the specific study. Some trials may last for a few weeks, while others can extend over several months or even years. The number of visits required can also vary—some trials might necessitate daily visits, while others may only require monthly check-ins. All these details will be clearly outlined in the study’s design, and our team will discuss them with you during the initial consultation.