Informations générales (source: ClinicalTrials.gov)
New Perioperative and Non-pharmacological Practices in Endometriosis at the Crossroad of Gynecology and Chronic Pain (EndoDOL)
Interventional
N/A
Hospices Civils de Lyon (Voir sur ClinicalTrials)
décembre 2019
juin 2026
29 juin 2024
Endometriosis is a condition affecting about 10% of childbearing age women. It can begin
a few months to a few years after puberty. It causes abdominal and pelvic pain that can
be extremely debilitating, affecting the quality of patients life by affecting sexuality
and fertility. Psychological repercussions are very important and underestimated. Patient
care focuses most often on the "organ pathology treatment ".
This study proposes to evaluate a multidisciplinary patient care by insisting on
anatomo-physiological pain management, psychological and bodily, in the perioperative
phase.
The main objective is to evaluate benefit of psychological and corporal group management
on the overall quality of life of patients with severe endometriosis in terms of
endometriotic damage and/or functional and painful repercussions, requiring surgery,
before or after this study
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| Croix Rousse Hospital - 69004 - Lyon - France | Patricia Branche, MD | Contact (sur clinicalTrials) | |||
Critères
Femme
Inclusion Criteria:
- Patients >=18 years
- Patients with deep endometriosis according to the CNGOF (collège national des
Gynécologues et Obstétriciens Français) and/or chronic pain related to endometriosis
according to doctor's evaluation and to the definitions of IASP (International
Association for the Study of Pain) and HAS (French National Authority for Health) in
treatment failure despite appropriate medical or surgical management of
endometriosis
- Patients with social security
- Patients willing to come to all study visits
- Patients who signed their informed consent
- Patients >=18 years
- Patients with deep endometriosis according to the CNGOF (collège national des
Gynécologues et Obstétriciens Français) and/or chronic pain related to endometriosis
according to doctor's evaluation and to the definitions of IASP (International
Association for the Study of Pain) and HAS (French National Authority for Health) in
treatment failure despite appropriate medical or surgical management of
endometriosis
- Patients with social security
- Patients willing to come to all study visits
- Patients who signed their informed consent
- Patients unable to participate in group care:
- Patients with social phobia assessed during the inclusion interview
- Patients with psychiatric disorders of a psychotic nature: delirium,
hallucination, incoherent thoughts
- Patients with behavioral disorders of hetero-aggressive or self-aggressive type
oPatients with a handicap that prevents them following the physical and
psychological group sessions (speech disorders, hearing, visual or practical)
- Pregnant women
- Patients planning a change (stop, start) during the study of their psychological
management in their current care path.
- Patients planning a change (stop, start) during the study of their treatment by
non-medicinal techniques (auriculo-acupuncture, relaxation and self-hypnosis,
transcutaneous neurostimulation by TENS)
- Patients suffering from other severe or chronic somatic diseases associated with
endometriosis
- Patients with cognitive disorders
- Patients with analgesics addiction (psychoactive substances, morphine substances,
etc.)
- Patients protected by law (under guardianship / trusteeship)
- Patients participating in another interventional research that may interfere with
the protocol results