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Evaluation of the Effect of Lactobacilli on Pain Relief in Endometriosis

Evaluation of the Effect of Administration of Lactobacilli on Pain Relief in Endometriosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150819023684N5
Enrollment
30
Registered
2018-04-17
Start date
2016-11-21
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Endometriosis. Endometriosis

Interventions

Intervention 1: Intervention Group: Lactobacilli tablets, once daily with the trade name "Lactofem" from Zist Takhmir Pharmaceutical Company which contains 10 to the power 9 colony count of the follow
daily 1 tablet of the placebo which is made by the pharmaceutical company Zist Takhmir with the exactly same packaging and appearance with "Lactofem". The tablet will be taken for 8 weeks and the pa

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Mean VAS score. Timepoint: 8 and 12 weeks after starting of drug use. Method of measurement: VAS Questionnaire.

Secondary

MeasureTime frame
Drug Adverse Effects. Timepoint: 8 and 12 Weeks after starting drug use. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Sepideh Khodaverdi

Iran University of Medical Sciences

sepidehkhodaverdi@yahoo.com+98 21 6435 2562

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 20, 2026