NCT06239051

Brief 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. Anonymized patients data about clinical procedures are used, taken from the internal database of the Humanitas fertility center

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
136

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Sep 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 18, 2023

Completed
6 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 24, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 24, 2023

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

January 26, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 2, 2024

Completed
Last Updated

February 2, 2024

Status Verified

January 1, 2024

Enrollment Period

6 days

First QC Date

January 26, 2024

Last Update Submit

January 26, 2024

Conditions

SustainabilityFemale Infertility

Outcome Measures

Primary Outcomes (1)

  • 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

    From 18th September 2023 to 24th September 2023

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
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.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

Istituto Clinico Humanitas

Rozzano, Milano, 20089, Italy

Location

MeSH Terms

Conditions

Infertility, Female

Condition Hierarchy (Ancestors)

Genital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesInfertility

Study Officials

  • Michele Tedeschi

    Humanitas Research Hospital IRCCS, Rozzano-Milan

    STUDY CHAIR

  • Paolo Emanuele Levi Setti

    Humanitas Research Hospital IRCCS, Rozzano-Milan

    STUDY DIRECTOR

  • Camilla Ronchetti

    Humanitas Research Hospital IRCCS, Rozzano-Milan

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 26, 2024

First Posted

February 2, 2024

Study Start

September 18, 2023

Primary Completion

September 24, 2023

Study Completion

September 24, 2023

Last Updated

February 2, 2024

Record last verified: 2024-01

Locations

IT(1)