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An exploratory trial about the efficacy of lactobacillus A and substance B on endometriosis

An exploratory trial about the efficacy of lactobacillus A and substance B on endometriosis - An exploratory trial about the efficacy of lactobacillus A and substance B on endometriosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000017530
Enrollment
30
Registered
2015-05-31
Start date
2015-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

endometriosis

Interventions

combination drug is administarated for 3 months single drug is administarated for 3 months

Sponsors

The University of Tokyo Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1 patients who obtained the diagnosis of endometriosis 1-1 Past history of operation for endometriosis. diagnosed pathologically or surgical findings with the observation at the operation. 1-2 The patient diagnosed endometriosis by an internal exam or ultrasound exam 2 The menstrual cycle is within 25-31days low dose EP is unconcerned. 3 Use at least one dose of painkiller dualing the time of menstrual periods.

Exclusion criteria

Exclusion criteria: 1) have severe asthma or allergy to multiple drugs 2) has diarrhea by uptake of dairy goods 3) have past history of allergy to dairy products 4) cervical cytology worse than class 2 5) have carcinoma 6) severe hepatic or renal damage or have past history of cardiac infarct 7) past history of hepatitis 8) severe anemia 9) appropriate judged by responsible doctor

Design outcomes

Primary

MeasureTime frame
Pain is assessed with VAS. The average score of menstrual pain when combination drug is used is compared with that of menstrual pain when single drug is used

Countries

Japan

Contacts

Public ContactTAKAMURA MASASHI

University of Tokyo Obstetrics and Gynecology

takamura-tky@umin.ac.jp03-3815-5411

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026