SustainabilityGreenNCT06239051
Greening the Humanitas Fertility Center: How to Build a More Sustainable Medical Daily Routine
An observational study of Sustainability and Female Infertility, run by Istituto Clinico Humanitas at 1 site in Italy.
Trial summary
The goal of this observational study is to redefine an everyday clinical routine at the Humanitas Fertility center calculating the effects derived from the reduction of inappropriate and avoidable tests, procedures, tools and treatments currently used. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women only
- Conditions the study is for
- Sustainability, Female Infertility
- How many people
- 136 participants
- Where
- 1 siteItaly
- Study dates
- 18 Sep 2023to 24 Sep 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 45 years
- Women only
- No healthy volunteers
- Adult
Study population: All outpatient, surgical and laboratory procedures, considered as daily clinical routine at the Humanitas Fertility center, will be taken into account, analysed and defined as appropriate or not.
All outpatient, surgical and laboratory procedures, considered as daily clinical routine at the Humanitas Fertility center, will be taken into account, analysed and defined as appropriate or not.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Humanitas Fertility Center: The Green (R)Evolution
The goal of this observational study is to redefine an everyday clinical routine at the Humanitas Fertility center calculating the effects derived from the reduction of inappropriate and avoidable tests, procedures, tools and treatments currently used.
Anonymized patients data about clinical procedures are used, taken from the internal database of the Humanitas fertility center
- Conditions
- Sustainability, Female Infertility
- Medical subject headings
- Infertility, Female
What is being measured
The primary outcome is the main question the study is designed to answer.
Reduction of avoidable procedures and assessment of its enviromental impact
Redefine an everyday clinical routine at the Humanitas Fertility center, calculating the effects derived from the reduction of inappropriate and avoidable tests, procedures, tools and treatments currently used
Measured: From 18th September 2023 to 24th September 2023
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Feb 2024
- Study start18 Sep 2023
- Primary completion24 Sep 2023
- Study completion24 Sep 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SustainabilityStudies of the same condition, open and under way.
- More trials run by Istituto Clinico HumanitasThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Ecologic or community
- Time perspective
- Retrospective
- Enrolment
- 136 participants (actual)
Sponsor and investigators
- Lead sponsor
- Istituto Clinico Humanitas
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Michele Tedeschi, Study chair, Humanitas Research Hospital IRCCS, Rozzano-MilanPaolo Emanuele Levi Setti, Study director, Humanitas Research Hospital IRCCS, Rozzano-MilanCamilla Ronchetti, Principal investigator, Humanitas Research Hospital IRCCS, Rozzano-Milan
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06239051
- Sponsor's protocol ID
- Green Project
- Acronym
- Green
- Status last verified
- Jan 2024
- First submitted
- 26 Jan 2024
- Last updated
- 2 Feb 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Humanitas Fertility Center: The Green (R)Evolution
- ClinicalTrials.gov ID
- NCT06239051
- Acronym / sponsor ID
- Green / Green Project
- Conditions
- Sustainability, Female Infertility
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 136 participants (actual)
- Lead sponsor
- Istituto Clinico HumanitasUniversity, hospital or other
- Study start
- 18 Sep 2023 (actual)
- Primary completion
- 24 Sep 2023 (actual)
- Study completion
- 24 Sep 2023 (actual)
- First posted
- 2 Feb 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational study is to redefine an everyday clinical routine at the Humanitas Fertility center calculating the effects derived from the reduction of inappropriate and avoidable tests, procedures, tools and treatments currently used.
Anonymized patients data about clinical procedures are used, taken from the internal database of the Humanitas fertility center
Study design
- Observational model
- Ecologic or community
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- All outpatient, surgical and laboratory procedures, considered as daily clinical routine at the Humanitas Fertility center, will be taken into account, analysed and defined as appropriate or not.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Reduction of avoidable procedures and assessment of its enviromental impact
Time frame: From 18th September 2023 to 24th September 2023
Redefine an everyday clinical routine at the Humanitas Fertility center, calculating the effects derived from the reduction of inappropriate and avoidable tests, procedures, tools and treatments currently used
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Feb 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Michele Tedeschi study chair
Humanitas Research Hospital IRCCS, Rozzano-Milan
Paolo Emanuele Levi Setti study director
Humanitas Research Hospital IRCCS, Rozzano-Milan
Camilla Ronchetti principal investigator
Humanitas Research Hospital IRCCS, Rozzano-Milan
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Sustainability and Female Infertility, run by Istituto Clinico Humanitas at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 2 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Reduction of avoidable procedures and assessment of its enviromental impact (time frame: From 18th September 2023 to 24th September 2023). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2024.