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NCT05468593Completed

Patient Outcomes After Hepatic Artery Infusion Pump Placement

Patient Reported Outcomes After Hepatic Artery Infusion Pump Placement

Source: ClinicalTrials.gov · Last updated 30 Jul 2024

Brief summary (registry, in English)

The purpose of this study is to evaluate the surgical outcomes and the quality of life (QOL) in patients undergoing hepatic artery infusion pump placement for colorectal liver metastases (CRLM).

Status (registry)
Completed
Study type
Observational
Enrollment
12 (actual)
First submitted
12 Jul 2022
Start date
12 Jul 2022
Primary completion date
1 Jul 2024
Lead sponsor
Mayo Clinic
NCT number
NCT05468593

What you commit to

  • Study type: Observational
  • Participants enrolled: 12
  • From 12 Jul 2022 to the primary completion date, 1 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Systemic disease.

Other

  • Absence of written consent.
  • Pregnancy.

Who the study is looking for

  • Patients who receive a Hepatic Artery Infusion Pump at Mayo Clinic Rochester for liver metastases from colorectal cancer.
  • Written consent.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic - Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.