Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
4079 participants
OBSERVATIONAL
2023-01-01
2024-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of a Multi-strain Oral Probiotic on the Vaginal Microbiota Composition in Healthy Women and Women with Endometriosis
NCT06592976
Exposure to Persistent Organic Pollutants and Severity of Endometriosis in the ComPaRe-Endometriosis Cohort
NCT06973603
The Effect of the Self-Care Support Program on Women With Endometriosis
NCT05861739
Establishment of the Human Intestinal and Salivary Microbiota Biobank - Gynecological Diseases
NCT04698109
A Study on the Correlation Between Endometriosis and Intra-tissue Microbiota
NCT06266897
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Administration of antibiotics in the last 15 days prior to entry into the study or indications for antibiotic prophylaxis.
* Orthodontic Appliances.
* Immunological diseases or use of drugs that can affect oral tissues (phenytoin, cyclosporine), nifedipine, chronic use of nonsteroidal anti-inflammatory drugs.
* Refusal to participate in the study.
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Bari Aldo Moro
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Giuseppe D'Albis
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Saverio Capodiferro, Professor
Role: STUDY_DIRECTOR
University of Bari Aldo Moro
Massimo Corsalini, Professor
Role: STUDY_DIRECTOR
University of Bari Aldo Moro
Giuseppe D'Albis
Role: PRINCIPAL_INVESTIGATOR
University of Bari Aldo Moro
Agneta Maria Teresa
Role: PRINCIPAL_INVESTIGATOR
University of Bari Aldo Moro
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Bari Aldo Moro
Bari, , Italy
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
endometriosis-oralhealt
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.