Dermatology clinical trials

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Dermatology
clinical trials

One of the main challenges in dermatology clinical trials is the glaring gap in effective questionnaires known as Patient-Reported Outcomes (PROs) and Observer-Reported Outcomes (ObsROs) to capture accurately the patient experience and that of their families.

Patients’ families are also significantly affected indirectly by the patient experience: patients with dermatological diseases endure more than skin suffering, and can face high levels of psychological distress.
The current landscape of dermatology clinical trials highlights the urgent need for stronger PROs, as existing measures are often too generic or miss the mark on specific patient concerns.

By prioritizing data capture through comprehensive PROs and ObsROs, we aim to ensure that our clinical trials not only measure treatment efficacy but also take into account the quality of life for patients and their families.

Collect meaningful data from patients and families with a direct impact on treatment outcomes

Our advisory board and eCOA experts provide comprehensive support in defining clinical endpoints, selecting PRO and ObsRO instruments, optimizing the frequency of questionnaires, and ensuring that our trials enhance the quality of life for patients and their families.
We understand the importance of not overwhelming patients and their families through excessive data collection. Our eCOA strategy emphasizes collecting only essential information that has a direct impact on treatment outcomes and quality of life, minimizing the patient burden while maximizing the relevance and utility of the data collected.
Patient engagement features are key. Because patients’ data are fundamental to clinical trials, it is important for patients to feel involved in the study. Thanks to co-created patient material, patients will understand their role and their responsibilities and will feel more engaged.

Capture essential trial data smoothly with our user-friendly eCOA solution

A large set of data collection modes are available to fit your dermatology study needs. With solutions such as ergonomic provisioned devices or BYOD you will always have a range of suitable options to propose to patients, caregivers, and clinicians.
With our efficient score calculation and real time reporting, clinicians will have direct and instant access to our Clin’form WebPortal to easily monitor clinical data and patient compliance in a timely manner.
We provide high quality data management throughout your dermatology clinical trial. Experienced data managers and programmers are involved from the beginning of the study and will manage the specifics of the questionnaires and the implementation of all the relevant edit checks, triggers, and alerts to facilitate use and compliance.