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Evaluation of Genetic Signature in Endometriosis Disease by Non Invasive Sampling

Evaluation of Genetic Signature in Endometriosis Disease by Non Invasive Sampling

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06100471
Acronym
niEndometriosi
Enrollment
150
Registered
2023-10-25
Start date
2023-05-01
Completion date
2024-12-31
Last updated
2024-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis, Hypofertility

Keywords

endo

Brief summary

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.

Detailed description

Retrospective selection based on anamnestic criteria of: 50 patients with diagnosed endometriotic adnexal pathology (case, CA), 50 patients with non-endometriotic adnexal pathology (control, CO) and 50 patients with no gynecological pathology, not undergoing surgery (analytical control). The study involves collecting a saliva sample from all patients involved in the study, and performing a biopsy from both patients with endometriotic adnexal pathology (CA) and patients with non-endometriotic adnexal pathology (CO).

Interventions

OTHERObservational study

Observational study in different tissues in identifing new genetic markers related to endometriosis disease

Sponsors

Eurofins Genoma
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Case population (CA), patients with endometriotic adnexal pathology * Control population (CO), patients with non-endometriotic adnexal pathology * Analytical control population (C-), patients with no gynecologic pathology, not undergoing surgery

Exclusion criteria

* Women with ages outside the inclusion range * Pregnant patient * Patient with a personal history of cancer * Patient infected with HIV

Design outcomes

Primary

MeasureTime frameDescription
Next Generation Sequencing technical validation1 monthAssessing the quality of Next Generation Sequencing via the FASTQC tool. Following benchmarks will be considered: 1.1 Per base sequence quality \[Phred score: positive real number, the higher the better\] 1.2 Total number of sequenced reads \[integer: positiver integer number, the higher the better\]
Wet lab kit validation1 monthAssessing the quality of the kit by mapping the reads against public miRNA databases. Following benchmark will be considered: Total reads mapped \[integer\]

Secondary

MeasureTime frameDescription
Tissue validation2 monthsGenetic profiling of miRNOME from saliva versus FFPE-tissues
Clinical validation4 monthsCorrelation of miRNOME signature in saliva among cases, controls and analytical groups
Biomarkers identification7 monthsIdentification of specific signature related to endometriosis, with at least 2 Log2fold change

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026