Greening the Humanitas Fertility Center: How to Build a More Sustainable Medical Daily Routine
NCT ID: NCT06239051
Last Updated: 2024-02-02
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
136 participants
OBSERVATIONAL
2023-09-18
2023-09-24
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Anonymized patients data about clinical procedures are used, taken from the internal database of the Humanitas fertility center
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Retrospective Trial on Low Prognosis Infertile Patients
NCT03290911
Desogestrel Versus GnRH Antagonist in IVF/ICSI
NCT04728659
Efficacy and Safety of Fertility Treatments and Fertility Preservation
NCT04602962
Drop-out of Infertile Couples: a Large Single Center Experience Over 10 Years
NCT06344585
To Investigate the Cumulative Live Birth Rates Using GnRH Antagonist or Agonist Protocol for COS in ART Treatment
NCT04026282
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.
ECOLOGIC_OR_COMMUNITY
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
18 Years
45 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istituto Clinico Humanitas
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Michele Tedeschi
Role: STUDY_CHAIR
Humanitas Research Hospital IRCCS, Rozzano-Milan
Paolo Emanuele Levi Setti
Role: STUDY_DIRECTOR
Humanitas Research Hospital IRCCS, Rozzano-Milan
Camilla Ronchetti
Role: PRINCIPAL_INVESTIGATOR
Humanitas Research Hospital IRCCS, Rozzano-Milan
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Istituto Clinico Humanitas
Rozzano, Milano, 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.
Green Project
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.