

Clinical Research Excellence at ICLS
A dedicated research team led by world-class experts Dr. Sheetal Sapra and Dr. Julie Khanna, trusted by the GTA community for over 30 years.
PATIENT-FIRST APPROACH
Advancing Care Through Research
For over 30 years, ICLS has been a trusted name in dermatology, plastic surgery, and clinical research. With more than 400,000 patients treated, our dedicated research team provides access to new treatments and technologies before they become widely available. Every study is conducted with a patient-first approach, prioritizing safety, innovation, and expert medical oversight.


Clinical Research Studies
Which Clinical Trial Are You Qualified for?
The Centre for Clinical Trials by ICLS conducts both original research and clinical trials alongside the pharmaceutical industry with the goal of bringing new treatment options to our patients. Our areas of skin research include but are not limited to acne, alopecia, eczema, psoriasis, rosacea, vitiligo and cosmetic studies.
5 Available Research Studies:
- Psoriasis
- Atopic Dermatitis
- Alopecia Areta
- Vitiligo
- Acne Scarring
Select Clinical Trial of Interest
Click the dropdown below to learn more about our trials and apply
Psoriasis
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Atopic Dermatitis
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Alopecia Areata
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Vitiligo
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Acne Scarring
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Oakville, Ontario
Serving the GTA Community for Over 30 Years
Trusted by Over 400,000 Patients and Counting.
ICLS has been a trusted leader in the GTA medical community for over 30 years, offering advanced treatments and pioneering clinical research. Led by Dr. Sheetal Sapra and Dr. Julie Khanna, our team of medical experts provides patients with access to cutting-edge treatments in a safe, professional environment.


Safety First. Trust Earned. Respect Always. Professionalism at Every Step.

Meet Our Team
Our Doctors

Dr. Sheetal Sapra
Dr. Sheetal Sapra is a pioneer in dermatology, known for advancing cutting-edge laser technologies and innovative treatments. As the Director of Dermatology and founder of the Centre for Clinical Trials at ICLS, he leads groundbreaking research and clinical trials, shaping the future of skincare and medical aesthetics.

Dr. Julie Khanna
Dr. Julie Khanna is a leading cosmetic plastic surgeon with over 25 years of experience, known for her patient-first approach and tailor-made solutions that align with each individual's goals.
Our Research Team

Avery
Clinical Research Coordinator

Sylvia
Clinical Research Assistant

Minuki
Clinical Research Assistant

Harmeet
Clinical Research Coordinator
FAQ
General Information About Clinical Trials
Clinical trials are research studies performed in people that are aimed at evaluating a medical intervention. They are the primary way that researchers find out if a new treatment, like a new drug or medical device is safe and effective in people. Often a clinical trial is used to learn if a new treatment is more effective and/or has less harmful side effects than the standard treatment.
The length of a clinical study varies, depending on what is being studied. Participants are told how long the study will last before they enroll.
Eligibility & Partcipation
Clinical trials have standards outlining who can participate called eligibility criteria. The clinical research coordinator you meet with will review all of these criteria to see if the clinical trial you are interested in is right for you.
Eligibility & Outcomes
Clinical trials are designed to determine if a treatment works, if it works better than other treatments and/or if it has side effects. They also provide important information on the cost-effectiveness of a treatment, the clinical value of a diagnostic test and how a treatment improves quality of life. While most clinical studies provide participants with medical products or interventions related to the illness or condition being studied, they do notprovide extended or complete health care, nor do they guarantee results.
Participants may withdraw from a study at any time, even if the study is not over. Ending participation early will not impact your ability to receive healthcare.
Compensation & Costs
No. You do not get paid to participate in a clinical trial, however, some trials do provide compensation per study visit for travel, childcare etc. Your study coordinator will review this with you.
Informed Consent & Risks
Informed consent is a process used by researchers to provide potential and enrolled participants with information about a clinical study. This information helps people decide whether they want to enroll or continue to participate in the study. The informed consent process is intended to protect participants and should provide enough information for a person to understand the risks of, potential benefits of, and alternatives to the study.
The risks related to study participation will be outlined in the informed consent form. Your study doctor will follow his/her standard medical decision-making process as well as follow any local guidance(s) available when deciding whether your participation and potential treatment is in your best interest.
COVID-19 Concerns
During the study, if you have tested positive or are under quarantine for suspected disease, please notify your study doctor right away. The study doctor will ask you about your symptoms, diagnosis and any treatment you may be receiving.
During your quarantine period your study visits will continue remotely until further notice. Your study doctor will discuss with the study Sponsor about what other steps should be taken.
Many studies have a remote study visit plan to accommodate for COVID-19. Your study coordinator will talk to you about this option.
The study doctor and staff will continue to follow local guidelines and practices to implement and ensure safety precautions and measures are in place, in order to protect both staff and patients.
When you arrive on site you will text or email the study coordinator you've been corresponding with to let them know you've arrived. Please wait in your car until you are asked to approach the main doors. You and any persons accompanying you must be wearing a mask to enter the building. You will be provided with hand sanitizer and you will have your temperature taken at the door. The research staff will be in frequent communication with you, in-particular before each study visit, to ensure you know what to expect upon your arrival and during your visit. They will let you know if anything has changed since your last visit, so that you know what to expect.
Please do not hesitate to raise any questions or concerns to our clinical coordinators.