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NCT06100471: niEndometriosi

Evaluation of Genetic Signature in Endometriosis Disease by Non Invasive Sampling

Status unknown Last updated 20 February 2024
What this trial tests

trial testing Observational study in Endometriosis in 150 participants. Status unknown.

Timeline
1 May 2023
Primary endpoint
31 July 2024
31 December 2024

Quick facts

Lead sponsorEurofins Genoma
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment150
Start date1 May 2023
Primary completion31 July 2024
Estimated completion31 December 2024
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Eurofins Genoma

Who can join

Adults 18 to 45, female only, with Endometriosis or Hypofertility. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Endometriosis is a disease that affects 10-15% of the general population and 50% of infertile women. It is characterized by the presence of endometrial tissue outside the uterine cavity. Endometriosis can lead to infertility by interfering through endocrine and mechanical alterations on the function of the ovaries, fallopian tubes, and uterus. The aim of the study is to define the differential expression of a cluster of RNAs tissue driven for the identification of an RNA profile in saliva, specific for endometriosis. This study focuses on the expression of genes involved in the control and regulation of apoptosis, cell survival, metabolism, cell adhesion and invasion, angiogenesis, inflammation, and estrogen receptor expression levels.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Observational study

Trials testing the same drug.

Other recruiting trials for Endometriosis

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06100471.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing