Clinical trial Recruiting at 1 site Observational Ages 18 and up

Reducing iodinated contrast in hospital wastewater using a dedicated urine collection device after CT scans

Official title: GREENWATER 2.0: Cutting Edge Solution for Reducing Iodinated Contrast Agents Via Post-Administration Collection Device

Run by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · NCT07620093 · Data updated 2026-11-12

This study tests whether using a special urine collection device after contrast CT scans can help recover iodinated contrast and reduce wastewater in adult outpatients.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment416 (estimated)
SponsorI.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Academic / other
Locations1 site (Milan, MI)
StatusRecruiting
StartedMarch 10, 2026
Main results expectedSeptember 2026
Study endsDecember 2026
Registry record updatedJune 24, 2026
Trial IDNCT07620093 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult patients (18+) scheduled for clinically indicated contrast-enhanced CT scans who can provide informed consent and are willing to wait ~60 minutes after contrast administration to use the urine collection device.

Probably not a fit

Patients who cannot use the urine collection device or who do not consent to post-contrast urine collection may not benefit from the approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

GREENWATER 2.0 is a single-center, prospective observational study in which adult outpatients undergoing clinically indicated contrast-enhanced CT scans use a dedicated urine collection device for about 60 minutes after injection. The study does not alter the imaging procedure, contrast agent, dose, or protocol; it only adds a post-scan urine collection step to measure how much contrast can be recovered and to assess patient acceptance. Primary questions focus on patient acceptance/compliance with post-contrast urine collection and the amount of iodinated contrast recovered from urine. Results will inform feasibility of integrating urine collection into radiology workflow to potentially reduce hospital wastewater contamination.

Why it matters

Potential benefit: If successful, this approach could enable recovery of iodinated contrast from urine and reduce environmental impact of hospital wastewater.

How similar studies have gone: The prior GREENWATER study indicated high patient willingness to participate in a post-contrast urine collection protocol, supporting feasibility but not proving environmental impact.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patients aged 18 years or older.
* Patients scheduled for a clinically indicated contrast-enhanced CT scan with iodinated contrast agent.
* Patients able to provide written informed consent.
* Patients willing to wait approximately 60 minutes after contrast injection before using the dedicated urine collection device.

Exclusion Criteria:

\- Patients unable to use the dedicated urine collection device for urine collection.

Where it's running

  • IRCCS Ospedale Galeazzi - Sant'Ambrogio
    Milan, Mi, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • How to prevent post-surgery skin infections in bedridden patients

    This study tests whether two cleaning methods for the skin of bedridden patients after major surgery can reduce skin bacteria more effectively than a standard sponge method.

    Recruiting I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Milan · NCT07848269

  • Metabolomics and Transcriptomics of Gliomas

    Researchers are testing whether metabolic and gene-expression profiles can reveal new glioma subgroups and improve models to study and develop treatments for IDH wildtype glioblastoma and IDH-mutant lower-grade gliomas.

    Recruiting I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Milan, Lombardy · NCT07832734

  • Femoral Component Alignment in Total Knee Replacement: Extramedullary vs Intramedullary Guidance

    This study tests whether an external (extramedullary) guide for placing the femoral component in knee replacement works as well as the traditional internal (intramedullary) guide.

    Recruiting I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Milan and 2 other locations · NCT07815080

  • Three nerve blocks for knee replacement: which one works best

    This trial tests three different nerve blocks used during knee replacement to see which provides the best pain relief for patients after surgery.

    Recruiting I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Milan, Italy and 1 other locations · NCT07751653

  • Falls risk in adults over 65: does asymmetry in legs matter for balance and safety

    This study tests whether differences between the two legs in strength or function help predict falls in adults 65 and older who move independently.

    Recruiting I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Milan, Milan · NCT07742397

  • Muscle Biomarkers and Early Management of Sarcopenia

    This trial tests a non-invasive ultrasound-based method to measure muscle quality and pairs it with a home exercise program to see if it can help people over 50 with sarcopenia or at risk for it.

    Recruiting I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio · Milan, Mi · NCT07692308

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.