Hidradenitis Suppurativa Biologic Trial Enrollment Form

Streamline Your Hidradenitis Suppurativa Clinical Trial Enrollment

Managing participant recruitment and consent for hidradenitis suppurativa (HS) biologic trials requires careful documentation of disease severity, medical history, and informed consent. This Hidradenitis Suppurativa Biologic Trial Enrollment Form provides a comprehensive, professional solution for research teams conducting clinical studies on this challenging dermatological condition.

Purpose-Built for HS Clinical Research

This template is designed specifically for dermatology research teams, clinical trial coordinators, and pharmaceutical researchers conducting biologic therapy trials for hidradenitis suppurativa. The form captures essential baseline data including Hurley staging, prior surgical interventions, current disease burden, and quality of life metrics—all critical for assessing treatment efficacy and participant eligibility.

Complete Participant Assessment in One Form

Rather than juggling multiple paper forms and consent documents, this digital template consolidates participant screening, medical history, disease severity assessment, quality of life evaluation, and informed consent into a single streamlined workflow. The structured format ensures consistent data collection across all participants while maintaining the professional standards required for clinical research.

HIPAA-Compliant Data Collection Made Simple

While Paperform itself is not HIPAA compliant, this template provides a solid foundation that can be adapted for use within your institution's compliant infrastructure. The form can be embedded into secure portals or used alongside your existing HIPAA-compliant systems to facilitate the enrollment process.

Automate Your Research Workflows with Stepper

Connect this form to Stepper to automatically route participant data to your research database, trigger coordinator notifications when new enrollments arrive, send automated follow-up reminders for baseline assessments, and create participant tracking records in your project management system—all without manual data entry.

Designed for Research Excellence

With conditional logic that adapts questions based on disease severity and treatment history, built-in consent documentation, and quality of life assessment tools, this template helps research teams maintain rigorous standards while providing a professional, accessible experience for study participants. Whether you're running a phase II trial or a long-term observational study, Paperform makes clinical research enrollment efficient and compliant.