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NCT04195438Completed

Postoperative Heme Oxygenase Induction and Carbon Monoxide Production as a Novel Method to Assess Hepatic Regeneration and Predict Hepatic Related Morbidity After Partial Hepatectomy

Postoperative Heme Oxygenase Induction and Carbon Monoxide Production as a Novel Method to Assess Hepatic Regeneration and Predict Hepatic Related Morbidity After Partial Hepatectomy-1301GCC

Source: ClinicalTrials.gov · Last updated 21 Jun 2024

Brief summary (registry, in English)

The study will monitor carbon monoxide production in patients undergoing liver resection. Carbon monoxide will be checked from arterial blood gas obtained routinely as a part of the postoperative care as well as from the exhaled air of the patient through a CO detector commercially available and used as smokerlyzer helping people to stop smoking. The results of the surgical resection will be collected from the patient routinely ordered tests after liver resection including pathology of the resected part of the liver, laboratory and radiology tests. The study aims to identify the relationship between CO production and recovery after liver resection. Results of this study may help in predicting and improving results of liver resection.

Status (registry)
Completed
Study type
Interventional
Enrollment
25 (actual)
First submitted
20 Nov 2019
Start date
7 May 2014
Primary completion date
26 Mar 2024
Lead sponsor
University of Maryland, Baltimore
NCT number
NCT04195438

What you commit to

  • Study type: Interventional
  • Participants enrolled: 25
  • From 7 May 2014 to the primary completion date, 26 Mar 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

  • Patients not having pathology proven liver malignancy

Age

  • Patients age less than 18

Other

  • Patient not able to comprehend or sign written consent form.

Who the study is looking for

  • Patients plan to have partial liver resection for primary liver pathology or metastatic disease.
  • Patients able to comprehend and willing to sign the written consent form.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

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
University of Maryland Baltimore Washington Medical Center
Coordinator of this site? Confirm its status
Glen BurnieUnited StatesUnknown status

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