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Tests diet advice and probiotics for pelvic pain in endometriosis and IBS

Tests diet guidance and Lactobacillus probiotics in women with endometriosis and irritable bowel syndrome.

Plain-language title generated from the registry record
Registry title: Impact of Dietary Guidance and Probiotics in the Treatment of Endometriosis and Irritable Bowel Syndrome in Women

Key facts

Where
Catanduva, BrazilSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 15 and 50 years old?

Source: NCT07149519, who can take part

Where in Brazil

  • Letícia Ferracini Lenharo HayashiCatanduva, BrazilTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of Sao Paulo
Trial code
NCT07149519
Record updated
2 September 2025
Original description
Patients with endometriosis are 2 to 3 times more likely to develop Irritable Bowel Syndrome (IBS) than women without the condition. IBS presents symptoms similar to those of intestinal and deep EDT, leading to diagnostic errors and delays in identifying such comorbidities. Diets have shown positive effects on symptoms in women with both conditions, supporting the theory of a similar pathophysiology. The investigators goal is to examine how dietary practices and probiotic use affect chronic pelvic pain in patients with both comorbidities.Read full original descriptionShow less

Impact of Dietary Guidance and Probiotics in the Treatment of Chronic Pelvic Pain Secondary to Endometriosis and Irritable Bowel Syndrome in Women: A Randomized, Double-Blind Clinical Trial

Patients with endometriosis are 2 to 3 times more likely to develop Irritable Bowel Syndrome (IBS) than women without the condition. IBS presents symptoms similar to those of intestinal and deep EDT, leading to diagnostic errors and delays in identifying such comorbidities. Diets have shown positive effects on symptoms in women with both conditions, supporting the theory of a similar pathophysiology. The investigators goal is to examine how dietary practices and probiotic use affect chronic pelvic pain in patients with both comorbidities.

Inclusion: Women between 18 and 50 years of age who wish to participate in the clinical trial; Willingness to voluntarily participate in the study and accept randomization to any of the three treatment arms; Participating exclusively in this clinical trial during the study period; Signing the Informed Consent Form (ICF) approved by the Research Ethics Committee (CEP) and CONEP.

Exclusion: Endometriosis requiring surgical treatment during the study period; Inability to use oral medication; Chronic, severe, or uncompensated clinical conditions, such as: malnutrition (BMI <18); insulin-dependent diabetes (types 1 or 2); uncontrolled hypertension; lung disease such as asthma or other chronic obstructive pulmonary disease; hematologic and liver diseases; advanced-stage chronic kidney disease (grades 3, 4, and 5); metabolic disorders; and immunosuppression; Clinical conditions of the gastrointestinal tract that cause IBS-like symptoms, such as: inflammatory bowel disease (Chron's disease, ulcerative colitis), microscopic colitis, celiac disease, and lactose intolerance; Severe eating disorders, such as: bulimia, anorexia nervosa, and binge-eating disorder; Chronic use of any medication with potential interaction with probiotics, the intestinal microbiota, or the natural progression of the disease in the last 6 months (such as probiotics, antibiotics, antifungals, antihistamines, digestive medications, or treatments for constipation or diarrhea); History of alcohol or drug dependence; Inability to cooperate with investigators due to cognitive impairment or mental state; Patients who already consume healthy foods or are on a restrictive diet more than four days a week, which may affect the evaluation results; Patients whose stool protopastological examination is altered; Pregnancy or lactation; Smoking in the last three years.

ClinicalTrials.gov NCT07149519