RecruitingNCT05928442

Interest of Salivary Signature of Endometriosis in the Heathcare Pathway of Adolescent

Interest of Salivary Signature of Endometriosis in the Heathcare Pathway of Adolescent - The ADOmiARN Study


Sponsor

ZIWIG

Enrollment

80 participants

Start Date

Jun 13, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

ADOmiARN is a multicentre, prospective, longitudinal, non-interventional, observational study carried out in obstetrics, gynecology and pediatrics departments in France and in Belgium. The main objective is to confirm the interest of the in vitro diagnostic medical device (EndoTest®) in adolescents with suspected endometriosis. The study population is made up of females aged 10 to 19 years with formally diagnosed endometriosis or suspected endometriosis. The patients concerned by the study are managed without any change in the care pathway, no any change in the therapeutic indications, no any change in the diagnostic examinations (imaging or biology) required according to the context, which are carried out in accordance with the national guidelines. 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 : * Collection of saliva * Completion of a self-questionnaire on symptom and quality-of-life.


Eligibility

Sex: FEMALEMin Age: 10 YearsMax Age: 19 Years

Inclusion Criteria8

  • Patient aged between 10 and 19 years,
  • Patient over 18 or legal representatives of patient under 18 who has dated and signed the consent form,
  • Patient with pelvic MRI available and conduct within 12 months prior to inclusion,
  • Patient from one of the 3 study populations:
  • A formal endometriosis diagnosed by clinical examination and imaging or
  • With prescription for coelioscopy because of a discrepancy between clinical and radiological findings or
  • A surgical indication for a pathology of the small pelvis other than endometriosis, in adolescents with suspected endometriosis faced with symptoms suggestive (dysmenorrhea, chronic or cyclic pelvic pain, urinary disorders cycle-dependent)
  • Patient affiliated to the healthcare system.

Exclusion Criteria8

  • Known pregnancy in progress,
  • Known infection with the human immunodeficiency virus (HIV),
  • Personal history of cancer,
  • Adolescent subject to a protective measure or placed adolescent,
  • Adolescent or her legal representatives presenting important difficulties in reading French language,
  • Patient or her legal representatives who have objected to the collection of her data,
  • Patient participating in an interventional study with drug or medical device or in the exclusion period of an interventional study
  • Patient who has participated or is participating in another study evaluating miRNA in endometriosis.

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Interventions

DEVICEin vitro diagnostic medical device

Collection of 2 saliva samples at inclusion.

BEHAVIORALCompletion of a self-questionnaire

Completion of a self-questionnaire on symptom and quality-of-life at inclusion.

DEVICEin vitro diagnostic medical device

Collection of 1 saliva sample at the follow-up visit.


Locations(13)

Hôpital de la Citadelle

Liège, Belgium

Centre chirurgical L'Avancée

Aix-en-Provence, France

CHU Angers

Angers, France

Clinique Tivoli-Ducos

Bordeaux, France

CHU Caen

Caen, France

AP-HM Hôpital de la Conception

Marseille, France

CHU Caremeau

Nîmes, France

Hôpital Tenon

Paris, France

APHP, Hôpital Cochin Port Royal

Paris, France

CHU Lyon Sud

Pierre-Bénite, France

CHU Rennes

Rennes, France

CHU Rouen

Rouen, France

Universitätsklinik für Frauenheilkunde, Inselspital Bern

Bern, Switzerland

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NCT05928442


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