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Clinical trials are systematic research studies designed to evaluate the safety, efficacy, and potential side effects of new medical treatments, drugs, or interventions in human participants. These trials follow strict protocols to gather scientifically sound data, often involving different phases.
Participants in clinical trials play a crucial role in expanding medical knowledge and improving patient care. It’s essential that individuals considering participation are well-informed about the potential benefits and risks, and that the trials adhere to ethical standards and regulations.
Our friendly staff will be more than happy to provide you with more information.
Some of the most common questions about Clinical Trials.
Clinical trials are carefully controlled research studies that evaluate the safety and effectiveness of new medical treatments, procedures, or devices. They help determine if these interventions are beneficial and should become standard practice.
Safety is the top priority in clinical trials. Extensive ethical guidelines and regulations govern their conduct. Participants are thoroughly informed about risks and benefits, and their consent is voluntary. Strict monitoring procedures and oversight committees ensure ongoing safety throughout the study.
Eligibility criteria vary depending on the trial and the condition being studied. Certain factors like age, medical history, and existing medications might affect eligibility. Checking clinical trial databases or consulting with your doctor can help you find relevant trials and assess your potential participation.
Benefits: Early access to potentially life-saving treatments, contributing to medical advancements, receiving expert medical care, and financial compensation in some cases.
Risks: Side effects from the investigational treatment, increased time commitment for appointments and tests, and the possibility of receiving a placebo (if applicable).
Note that these can vary depending on the clinical trial. Contact the team at Trident for more information
This depends on the specific trial design. It typically involves regular visits, tests, and procedures to monitor progress and assess the treatment's effects. The study team provides detailed information about the schedule and procedures beforehand.
Not all trials offer compensation, but some might reimburse expenses like travel or provide a stipend. Ensure you understand the financial aspects clearly before joining.
Participants have the right to withdraw at any time. The study team should discuss withdrawal procedures and ensure continued medical care if needed.
Strict confidentiality guidelines protect your privacy. Only authorized personnel involved in the research and regulatory monitoring will have access to your data.
Online databases like ClinicalTrials.gov and other resources specific to your condition or region can help you find relevant trials. Consult your doctor or healthcare provider for guidance.
Clinical trials are the cornerstone of medical progress. They provide the evidence needed to improve existing treatments and develop new therapies for various diseases. Participating in a trial contributes directly to advancing medical knowledge and improving healthcare outcomes for future generations.
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