Research Registration: Hyperemesis Gravidarum
Researchers engaged in any aspect of hyperemesis gravidarum (HG) are invited to register their studies with the International Collaboration on Hyperemesis Gravidarum (ICHG) network.
This registry supports the development of a global overview of current HG research activity and facilitates meaningful connections between researchers, clinicians, and patient advocates worldwide.
Purpose and Benefits of Registration
🧩 Enhanced Research Visibility
Registration enables the ICHG organisers to map ongoing HG research globally, identify overlaps and gaps, and promote potential synergies between investigators.
🧑⚕️ Access to International PPIE Infrastructure
Through the ICHG network, researchers may access experienced Patient and Public Involvement and Engagement (PPIE) contributors for support with study design, recruitment strategies, ethics processes, and dissemination plans.
🤝 Facilitated Collaboration
With your consent, we may connect you to other investigators, clinicians, or stakeholders whose interests align with your area of work. This includes invitations to collaborative initiatives, workshops, and relevant working groups.
🧠 Knowledge Exchange and Network Support
Registrants will receive occasional updates regarding international events, funding calls, and opportunities related to HG research, including the ICHG 2026 scientific programme.
🔒 Confidential and Research-Focused
The information you provide through this form will be stored securely and treated as strictly confidential. It will not be published or shared with external parties. If we identify a potential opportunity for collaboration or knowledge exchange based on your registration, we will contact you directly to request explicit permission before sharing any details with others in the network.