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.

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NOW RECRUITING

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.

On-site laboratory collection and processing
Trained nursing staff & clinical research staff
No Cost Associated With These Treatments
Access to cutting edge treatments & technologies

5 Available Research Studies:

  • Psoriasis
  • Atopic Dermatitis
  • Alopecia Areta
  • Vitiligo
  • Acne Scarring
On-site laboratory collection and processing
Trained nursing staff & clinical research staff
No Cost Associated With These Treatments
Access to cutting edge treatments & technologies

Select Clinical Trial of Interest

Click the dropdown below to learn more about our trials and apply

Psoriasis

"*" indicates required fields

Please fill out this form to see if you meet the requirements to qualify for our Psoriasis clinical trial.

1. How many handprints of psoriasis do you have on your face and body?*
Your privacy is our top priority. Your photos/videos are fully encrypted and will never be shared with anyone.
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    You may qualify for our Psoriasis clinical trial. Please fill out the rest of your contact information and we will get in touch with you.

    Accept Privacy Policy*

    Atopic Dermatitis

    "*" indicates required fields

    Please fill out this form to see if you meet the requirements to qualify for our Atopic Dermatitis clinical trial.

    1. How many handprints of Atopic Dermatitis do you have on your face and body?*
    Your privacy is our top priority. Your photos/videos are fully encrypted and will never be shared with anyone.
    Drop files here or
    Accepted file types: jpg, gif, png, jpeg, Max. file size: 10 MB, Max. files: 10.

      You may qualify for our Atopic Dermatitis clinical trial. Please fill out the rest of your contact information and we will get in touch with you.

      Accept Privacy Policy*

      Alopecia Areata

      "*" indicates required fields

      Please fill out this form to see if you meet the requirements to qualify for our Alopecia Areata clinical trial.

      1. Do you have hair loss on your scalp?*
      Your privacy is our top priority. Your photos/videos are fully encrypted and will never be shared with anyone.
      Drop files here or
      Accepted file types: jpg, gif, png, jpeg, Max. file size: 10 MB, Max. files: 10.

        You may qualify for our Alopecia Areata clinical trial. Please fill out the rest of your contact information and we will get in touch with you.

        Accept Privacy Policy*

        Vitiligo

        "*" indicates required fields

        Please fill out this form to see if you meet the requirements to qualify for our Vitiligo clinical trial.

        1. How many handprints of Vitiligo do you have on your face and body?*
        Your privacy is our top priority. Your photos/videos are fully encrypted and will never be shared with anyone.
        Drop files here or
        Accepted file types: jpg, gif, png, jpeg, Max. file size: 10 MB, Max. files: 10.

          You may qualify for our Vitiligo clinical trial. Please fill out the rest of your contact information and we will get in touch with you.

          Accept Privacy Policy*

          Acne Scarring

          "*" indicates required fields

          Please fill out this form to see if you meet the requirements to qualify for our Acne Scarring clinical trial.

          1. Do you have acne scarring present on both cheeks on your face?*
          Your privacy is our top priority. Your photos/videos are fully encrypted and will never be shared with anyone.
          Drop files here or
          Accepted file types: jpg, gif, png, jpeg, Max. file size: 10 MB, Max. files: 10.

            You may qualify for our Acne Scarring clinical trial. Please fill out the rest of your contact information and we will get in touch with you.

            Accept Privacy Policy*

            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.

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

            What is a clinical trial?

            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.

            How Long is a clinical Trial?

            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

            Who can participate in a clinical trial?

            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

            Is a clinical trial guaranteed to help me?

            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.

            What if I don't want to take part anymore?

            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

            Do I get paid to take part?

            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

            How do I learn the 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.

            Does participation in the study potentially put me at higher risk for COVID-19 infection?

            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

            How will my participation in the clinical trial be impacted in the event that at some point during my study participation, I test positive or I am being quarantined for suspected symptoms of COVID-19?

            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.

            What happens if I cannot attend an onsite study visit due to COVID-19?

            Many studies have a remote study visit plan to accommodate for COVID-19. Your study coordinator will talk to you about this option.

            Please explain what I should expect when I arrive onsite. Will the site have different requirements than in previous visits? Do I need to take any new precautions?

            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.

            Got Questions or Concerns?

            Get in Touch With Our Clinical Coordinators Today

            Send Us a Message