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Study identifier: NCT05514028 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: Active Not RecruitingOVAmiARN

Evaluation of Salivary RNAs in the Presence of an Adnexal Mass of Ovarian Origin

Condition: Ovarian Cancer · Ovarian Cyst Benign · Borderline Ovarian Cancer  ·  Sponsor: ZIWIG

PhaseN/A
Planned participants746
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where21 locations · 3 countries
For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

OVAmiARN is a multicentre, prospective, longitudinal, non-interventional, observational study carried out in 8 obstetrics and gynecology departments in France; in order to describe the evolution of salivary miRNA expression between the pre-operative and post-therapy visits according to the type of mass. In time, the clinical application will be to significantly reduce the time to diagnosis and improve the care pathway for ovarian adnexal mass. The study population consists of patients with an ovarian adnexal mass diagnosed by clinical examination and imaging (pelvic ultrasound and/or MRI) and requiring surgical management in routine care. The patients concerned by the study will be managed without modification of the care pathway, nor modification of the therapeutic indications, nor modification of the diagnostic or follow-up examinations (imaging or biology) necessary according to the context, which are carried out according to the recommendations of the HAS, CNGOF. In this study, the management and follow-up of patients : * Are not imposed by the study: the doctor remains free to make medical prescriptions (treatments and examinations) and to determine the interval between consultation visits, * Are not modified in comparison with the usual follow-up, except for the performance of the Collection of saliva

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

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Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patient over 18 years of age, * A patient with an ovarian adnexal mass diagnosed by clinical examination and imaging and likely to be ovarian cancer, a borderline tumour or a benign cyst, * Patient with an indication for surgery * Patient has dated and signed the consent form, * Patient affiliated to the healthcare system, Exclusion Criteria: * Pregnant patient * Patient infected with human immunodeficiency virus (HIV), * Patient with significant difficulties in reading or writing the French language. * Patient with another diagnosed cancer * Patient with a history of cancer less than 5 years old

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (21)

CHU de CaenCaen, Calvados, France
CGFLDijon, Côte d'Or, France
Institut BergoniéBordeaux, Gironde, France
CHU StrasbourgStrasbourg, Haut-Rhin, France
CHU ToulouseToulouse, Haute-Garonne, France
CHP St GrégoireSaint-Grégoire, Ille Et Villaine, France
Hôpital BICETRELe Kremlin-Bicêtre, Val de Marne, France
Institut Gustave RoussyVillejuif, Val de Marne, France
CHU AngersAngers, France
CH BastiaBastia, France
CHU Lyon Sud / Hospices Civils de LyonLyon, France
Centre Antoine LacassagneNice, France

+ 9 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

CaenDijonBordeauxStrasbourg

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