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Evaluation of miRNAs in Endometriosis (ENDOmiARN)

G

Groupe expert en endometriose-6 centre expert en endometriose

Status

Unknown

Conditions

Endometriosis Fertility
Endometriosis-related Pain
Endometriosis

Treatments

Other: Blood and salivar test

Study type

Observational

Funder types

Other

Identifiers

NCT04728152
n° Id-RCB 2020-A03297-32

Details and patient eligibility

About

We therefore propose a research project based on the prospective evaluation of miRNAs (blood and salivary) in patients with endometriosis diagnosed (by clinical examination and imaging) or suspected of endometriosis (clinical/radiological discordance) and in need of management in routine care (surgical or medical PMA) in the Endometriosis Expert Center Hospital.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 43 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient aged 18 to 43 years old,
  • Patient has dated and signed the consent form,
  • Patient affiliated with the French health care system,
  • Patients with formal endometriosis diagnosed by clinical examination and imaging or suspicion of endometriosis for which the diagnosis is a source of discrepancy between clinical and radiological data,
  • Patient with an indication for medically assisted procreation (MAP) or surgery validated in CPR (in routine care),
  • Patient who has had a pelvic MRI,
  • Patient who completed the symptom and quality of life questionnaires

Exclusion criteria

  • Pregnant patient,
  • Patient infected with the human immunodeficiency virus (HIV),
  • Patient with significant difficulties in reading or writing the French language,
  • Patient with a personal history of cancer,
  • Patient unable to comply with study and/or follow-up procedures,
  • Patient who has objected to the collection of her data.
  • Patient participating in another clinical research study.

Trial contacts and locations

1

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Central trial contact

EMILE DARAI, Prof; SOFIANE BENDIFALLAH, MD PHD

Data sourced from clinicaltrials.gov

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