← Eichor
Study identifier: NCT06615843 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Randomized Study of a Dematerialized Management for Post-Emergency Gynecological Follow-Up

Condition: Genital Diseases, Female · Ectopic Pregnancy · Uncertain Viability of Pregnancy  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants200
Who can joinFemale, 18 Years to 60 Years
Healthy volunteersNo

About this study

The GYNAB study aims to compare patient satisfaction and clinical outcomes between dematerialized post-emergency gynecological follow-up using a connected health app and traditional in-person follow-up. Conducted by Drs. Laëtitia CAMPIN and Louis MARCELLIN at Hôpital Cochin, it is sponsored by Assistance Publique - Hôpitaux de Paris. The main objective is to assess patient satisfaction at day 7 on a scale from 0 to 10, considering symptom management, follow-up quality, and task performance. Secondary objectives include comparing satisfaction at day 28, PROM-ED scores for symptom relief, understanding, reassurance, and care planning at days 7 and 28, hospitalization rates, unscheduled consultations, surgical interventions, total hospital time by day 28, and physician satisfaction at 28 days. This randomized trial involves women aged 18-60 needing follow-up for conditions like genital infections, non-complicated ectopic pregnancies, unlocated pregnancy, first trimester metrorrhagia, miscarriages , and severe vomiting before 12 weeks. Inclusion criteria are women aged 18-60 needing specified follow-up. Exclusion criteria are severe clinical intolerance, severe criteria ultrasound findings, non-French speakers, and inability to use digital applications. The intervention group uses a connected health app for data collection and communication, logging symptoms and test results, with medical team notifications for urgent updates. The control group receives traditional in-person foll…

This description comes directly from the study's public registry record.

Talk to the study team

Laetitia CAMPIN, MD  ·  33 015413680  ·  laetitia.campin@aphp.fr

Valérie PLENCE  ·  33 0158411178  ·  valerie.plence-fauroux@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Hôpital CochinParis, FranceRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06615843