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The Developmental Origins of Endometriosis

The Developmental Origins of Endometriosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05951452
Acronym
ENDOHaD
Enrollment
40
Registered
2023-07-19
Start date
2024-01-08
Completion date
2026-06-17
Last updated
2026-06-18

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

Conditions

Endometriosis

Keywords

Endometriosis, Testosterone, Oxytocin, DOHaD

Brief summary

Introduction: Endometriosis is a common pathology affecting one in 10 women, characterized by the ectopic development of endometrium, which can cause pain and/or infertility. This pathology is primarily determined by hereditary factors, but it is also susceptible to environmental influences, such as the age of the onset of menstruation or exposure to chemical substances that modify the endocrine system. Recent studies have highlighted that endometriosis is more common in women with relatively short ano-genital distances (AGD), and that sensitivity to pain is closely linked to adult levels of testosterone (T) or oxytocin (OT). Aim: The main objective is to compare the anogenital distance (AGD) between two groups of women: one with stage III or IV endometriosis (ENDO +) and another group without endometriosis confirmed by laparoscopy (ENDO -). The secondary objectives are to compare various factors between the 2 groups : * Basal testosterone levels in blood. * Variations in blood testosterone levels before and after a video stimulating empathy. * Basal oxytocin levels in saliva. * Variations in oxytocin levels in saliva before and after an empathy-stimulating video. * Pelvic pain, between D2 and D5 after the start of the menstrual cycle. For the ENDO + group only: * Evaluate patients' quality of life, between D2 and D5 after the start of the menstrual cycle. * Correlate pain experienced over the last 4 weeks with hormonal markers (AGD, T, OT). Methods: Participants in the ENDO+ group will fill in a questionnaire assessing the impact of pain experienced over the past 4 weeks on their quality of life. D0 is defined as the day when participants experience a menstrual bleed before 10 am. All participants will return for project-specific hospital appointment between D2 and D5 after the start of their menstrual cycle to measure T, Sex Hormone-Binding Globulin (SHBG) and OT. During this consultation, the following samples will be taken: * 10mL blood sample * 2mL saliva sample Both samples will be taken at t0 (before watching the video) and t1 (20 minutes after watching the video).

Interventions

OTHERBlood samples for testosterone and SHBG measurements

Several measurements of the testosterone concentration will be performed on serum from 10 mL of blood collected at: * t0 corresponding to the start of the hospital appointment and before watching the video * t1 which corresponds to 20 minutes after watching a 2 minutes empathy-inducing video

OTHERSaliva samples for oxytocin measurements

Several measurements of the oxytocin concentration will be performed on 2 ml saliva samples: * t0 corresponding to 20 minutes after the start of the hospital appointment and before watching the video * t1 which corresponds to 20 minutes after watching a 2 minutes empathy-inducing video

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER
Centre National de la Recherche Scientifique, France
CollaboratorOTHER
Fondation pour la Recherche sur l'Endométriose
CollaboratorUNKNOWN
Fondation pour la Recherche Médicale
CollaboratorOTHER
Université Montpellier
CollaboratorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 38 Years

Inclusion criteria

* Nulliparous woman * No hormonal contraception for at least 3 months * Regular menstrual cycles (between 26 and 32 days) or proven ovulation (positive urine ovulation test ovulation test or progesterone level \>3 ng/ml in the luteal phase) * Normal BMI (≥ 18,5 and \< 30 kg/m²) Specific criteria (ENDO+ group) : * Stage III or IV endometriosis confirmed by laparoscopy or by laparotomy or MRI * Painful symptoms Specific criteria (ENDO- group) : • Patient without endometriosis confirmed by laparoscopy

Exclusion criteria

* Ovarian stimulation planned within 3 months * Adenomyosis * Use of a copper coil * Polycystic ovary syndrome * Pudendal neuralgia * Episiotomy or lesion of the posterior perineum that may modify AGD * Diabetes or thyroid disease * Chronic liver failure, chronic renal failure, cardiac pathology, autoimmune disease * Autism * Diagnosis and/or treatment for psychiatric illness * Chronic exposure to cocaine, methamphetamine, morphine or ecstasy within 30 days before the inclusion visit * Chronic exposure to Tetrahydrocannabinol (THC) within 7 days prior to inclusion. * Patient on treatment(s) that vary oxytocin (e.g. atosiban), testosterone or GnRH * Pregnant or breast-feeding patient * Patients who have given birth or breastfed within 6 weeks before the inclusion visit * Patient unable to read French * Failure to obtain informed consent * Patient not affiliated with or not benefiting from a national health insurance scheme * Person under legal protection, guardianship or curatorship * Patient participating in other research involving the human person

Design outcomes

Primary

MeasureTime frameDescription
Measure of the anogenital distance (AGD)At diagnosis or at inclusionAGD is measured at enrollment for patients already diagnosed by Magnetic resonance imaging (MRI), and it is measured during the laparoscopy once the diagnosis has been confirmed. AGD is measured by 2 different operators with a millimetric precision ruler according 2 validated methods : * measure of the distance from the clitoral surface to the anus (AGD-AC), and * measure of the distance from the posterior fourchette to the anus (AGD-AF). The method is described here: https://www.jove.com/v/57912/ Each operator will measure the AGD-AC and the AGD-AF 3 times. For each type of AGD, the final value will correspond to the mean of the 6 values.

Secondary

MeasureTime frameDescription
Basal total testosteronet0 : Between the second and the fifth day of the menstrual cycle, before wathching an empathy-inducing videoThe basal total testosterone (Ttotal(t0)) level is measured in blood
Basal bio-available testosteronet0 : Between the second and the fifth day of the menstrual cycle, before wathching an empathy-inducing videoThe basal bio-available testosterone (Tbio-available(t0)) level is measured in blood
Basal sex hormone-binding globulint0 : Between the second and the fifth day of the menstrual cycle, before watching an empathy-inducing videoBasal sex hormone-binding globulin (SHBG(t0)) level is mesured in blood
Basal Free Androgen Indext0 : Between the second and the fifth day of the menstrual cycle, before watching an empathy-inducing videoBasal Free Androgen Index (FAI(t0)) = (Ttotal(t0)/SHBG(t0))\*100
Total testosterone after empathy inductiont1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoThe total testosterone level after empathy induction (Ttotal(t1)) is measured in blood
Bio-available testosterone after empathy inductiont1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoThe bio-available testosterone level after empathy induction (Tbio-available(t1)) is measured in blood
Sex hormone-binding globulin after empathy inductiont1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoSex hormone-binding globulin after empathy induction (SHBG(t1)) is mesured in blood
Free Androgen Index after empathy inductiont1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoFree Androgen Index after empathy induction (FAI(t1)) = (Ttotal(t1)/SHBG(t1))\*100
Variation in total testosterone levels before and after an empathy-inducing videot1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoThe level of variation in total testosterone before (t0) and after watching empathy-inducing video (t1) is assessed according to: Ttotal(t1)-Ttotal(t0)
Variation in bio-available testosterone levels before and after an empathy-inducing videot1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoThe level of variation in bio-available testosterone before (t0) and after watching empathy-inducing video (t1) is assessed according to: Tbio-available(t1)-Tbio-available(t0)
Variation in Sex hormone-binding globulin levels before and after an empathy-inducing videot1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoThe level of variation in Sex hormone-binding globulin before (t0) and after watching empathy-inducing video (t1) is assessed according to: SHBG(t1)-SHBG(t0)
% of variation in Free Androgen Index before and after an empathy-inducing videot1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing video% of variation in Free Androgen Index before (t0) and after watching empathy-inducing video (t1) is assessed according to: \[\[FAI(t1)-FAI(t0)\]/FAI(t0)\] × 100
Basal oxytocin (OT) levelt0 : Between the second and the fifth day of the menstrual cycle, before wathching an empathy-inducing videoThe basal OT level is measured by the dosage in the saliva of : Total OT (OTtotal(t0))
Oxytocin (OT) level after empathy inductiont1 : Between the second and the fifth day of the menstrual cycle, after wathching an empathy-inducing videoThe basal OT level is measured by the dosage in the saliva of : Total OT (OTtotal(t1))
Variation in oxytocin (OT) level before and after an empathy-inducing videot1 : Between the second and the fifth day of the menstrual cycle, after wathching empathy-inducing videoVariation in OT level before (t0) and after watching an empathy-inducing video (t1) is assessed in the saliva according to: \- OTtotal(t1)-OTtotal(t0) -% of variation of OT = \[\[OT(t1)-OT(t0)\]/OT(t0)\] × 100
Area under the Receiving Operator Characteristic (ROC) curve for AGDAt diagnosis (ENDO+) or at enrollment (ENDO-)The ROC curve is a graphical representation that illustrates the performance of a binary classification model. It plots the true positive rate (sensitivity) against the false positive rate (1 - specificity) at various classification thresholds. In other words, the model's sensitivity corresponds to the model's ability to detect patients (ENDO+) while the model's specificity corresponds to the model's ability to detect a non-patient (ENDO-). The ROC curve helps assess the model's ability to correctly identify true positives while minimizing false positives. The area under the ROC curve (AUC) can be interpreted as the probability that, among two randomly chosen subjects, a patient and a non-patient, the value of the marker is higher for the patient than for the non-sick. An AUC of 0.5 (50%) indicates that the marker is non-informative. An increase in AUC indicates an improvement in discriminatory abilities, with a maximum of 1.0 (100%).
Pelvic pain intensityt0 : Between the second and the fifth day of the menstrual cycle, before watching an empathy-inducing videoPelvic pain will be assessed using a Visual Analogue Scale (VAS). The visual analog scale (VAS) is a validated, unidimensional subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain."

Countries

France

Contacts

STUDY_CHAIRAlexandra ALVERGNE, PhD

Centre National de la Recherche Scientifique, France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 19, 2026