Faq’s

A clinical trial is a research study that involves human participants to evaluate new medical treatments, drugs, devices, or procedures. These trials are essential for determining the safety and effectiveness of new therapies before they become widely available.

Participating in a clinical trial gives you the opportunity to contribute to medical advancements that can benefit future patients. Additionally, you may gain access to cutting-edge treatments not yet available to the public. Some participants also find satisfaction in being closely monitored and cared for by a medical team throughout the study.

Each trial has specific eligibility criteria based on factors such as age, gender, medical history, and current health status. These criteria ensure that the study results are accurate and reliable. Our team will review your medical history and discuss your eligibility with you.

All clinical trials conducted by Latnus Clinical Research adhere to strict safety guidelines. Our studies are overseen by Institutional Review Boards (IRBs) to ensure that the rights and safety of participants are protected. Additionally, trials follow Good Clinical Practice (GCP) standards, which are international ethical and scientific quality guidelines.

Many clinical trials offer compensation for your time and travel expenses. Compensation varies depending on the specific study. Our team will provide detailed information about compensation before you agree to participate.

If you experience any side effects during the trial, you should inform our medical team immediately. Your safety is our top priority, and we will closely monitor your health throughout the study. If necessary, adjustments will be made, or you may be withdrawn from the study to protect your well-being.

Yes, participation in a clinical trial is completely voluntary. You can withdraw from the study at any time, for any reason. Your decision to leave will not affect your relationship with your healthcare provider or access to future medical care.

The duration of clinical trials varies depending on the type of study and its objectives. Some trials may last a few weeks, while others may continue for several months or even years. Before enrolling, you will be informed of the expected duration and time commitment.

Clinical trials are conducted in four phases:

• Phase I: Focuses on safety and dosage in a small group of participants.
• Phase II: Explores the effectiveness of the treatment while continuing to monitor safety in a larger group.
• Phase III: Confirms effectiveness, monitors side effects, and compares the new treatment to current standard treatments in a large population.
• Phase IV: Takes place after FDA approval to gather more information on the treatment’s long-term effects and safety in a broader population.

As a clinical trial participant, you have the right to:

• Be fully informed about the study, including potential risks and benefits.
• Ask questions at any time.
• Receive medical care throughout the trial.
• Withdraw from the trial at any time, without penalty or loss of benefits.
• Have your personal information kept confidential.