ClinicalTrials.Veeva

Menu

Study of the Influence of the Mediterranean Diet on the Quality of Life of Patients With Endometriosis.

B

Biogipuzkoa Health Research Institute

Status

Not yet enrolling

Conditions

Endometriosis

Treatments

Other: Diet supplementation

Study type

Interventional

Funder types

Other

Identifiers

NCT07270393
PAR-DON-2024-01

Details and patient eligibility

About

The severities of chronic disease symptoms correlate with the levels of analytical parameters of inflammation. Studies have been published in which the Mediterranean diet has an anti-inflammatory phenomenon, decreasing inflammation parameters. This decrease correlates with an improvement in symptoms.

Endometriosis is a chronic inflammatory disease and the influence of the Mediterranean diet on the decrease of inflammation parameters in women with endometriosis has been studied.

The studies carried out to assess whether this decrease in inflammatory parameters correlates with clinical improvement and quality of life in these patients have low/very low scientific evidence (small sample size, no control group) and with different interventions (diets, restrictions and/or supplements), which prevent their analysis as a whole.

Therefore, our hypothesis is that the Mediterranean diet, due to its anti-inflammatory effect, can improve the symptomatology and quality of life of patients with endometriosis.

Enrollment

104 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female.
  • Age 18-45.
  • Premenopausal status.
  • Radiological diagnosis (by transvaginal ultrasound and/or MRI) and/or surgical diagnosis of endometriosis.
  • Follow-up in the Gynecology Department of OSI Donostia (at least 1 visit in the last year).
  • Clinical score of at least 3/10 on the Numerical Scale in at least one symptom related to endometriosis).
  • Possibility of understanding Spanish.
  • Possibility of understanding the indicated dietary recommendations.
  • Acceptance of inclusion in clinical study, by signing informed consent.

Exclusion criteria

  • Diagnosis of Eating Disorder.
  • Diagnosis of malabsorptive syndromes: Chron's disease, Ulcerative colitis, short bowel syndrome, gastric by-pass, irritable bowel.
  • Other concomitant diseases that produce CPD.
  • Autoimmune diseases.-
  • Metabolic diseases requiring follow-up of specific diets.
  • Diagnosed gluten intolerance.
  • Vegan diet.
  • Follow-up by a nutritionist.
  • Diagnosis of severe mental illness requiring treatment.
  • Pregnancy or current breastfeeding.
  • Active cancer process.
  • Personal history of gynecologic or digestive oncologic process.
  • Change of treatment or surgery during follow-up.
  • Surgery related to endometriosis or change of treatment in the 6 weeks prior to enrollment in the study.
  • Drug abuse. Opioid analgesia < 3 months.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

104 participants in 2 patient groups

Control Group
No Intervention group
Description:
This group will not receive normocaloric Mediterranean diet recommendations.
Intervention Group
Experimental group
Description:
This group will receive a series of normocaloric Mediterranean diet recommendations.
Treatment:
Other: Diet supplementation

Trial contacts and locations

1

Loading...

Central trial contact

Jone Paredes Goenaga JONE.PAREDESGOENAGA@osakidetza.eus, Ginecology and Obstetrics

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems