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Evaluation of the Effect of Lactobacilli on Pain Relief in Endometriosis

Phase 3
Conditions
Endometriosis.
Endometriosis
Registration Number
IRCT20150819023684N5
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
30
Inclusion Criteria

Definitive diagnosis of endometriosis
Menstrual cycle in the range of 21-35 days
Aged 18-45 years
Those who had VAS (Visual Analogue Scale) Score intensity of 5 or more for their pain intensity
Passing at least 3 months and 1 year at the most since surgery

Exclusion Criteria

Patients who had received hormonal treatment during the past 3 months
History of liver or renal disease
history of carcinoma
Patients with history of diarrhea after consuming dairy products
Consumption of food or any type of probiotic product
Those who had a pain intensity of less than 5 according to the VAS Score
Patients who had received antibiotics during the past 3 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mean VAS score. Timepoint: 8 and 12 weeks after starting of drug use. Method of measurement: VAS Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Drug Adverse Effects. Timepoint: 8 and 12 Weeks after starting drug use. Method of measurement: Questionnaire.
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