Despite the severity of uterine rupture, research remains limited and fragmented. Most studies focus narrowly on the rupture itself, without capturing the wider picture of symptoms, patient background, or early warning signs.

Our international survey collects anonymised data from women who have experienced a complete uterine rupture or a partial rupture window or dehiscence. The goal is to better understand shared symptom profiles, risk contexts, and delays in recognition in order to improve prevention strategies and clinical care.

As responses accumulate, we publish publicly accessible reports that summarise current findings and support awareness and medical reflection.

Participation is voluntary, and all collected data is anonymised.