NCT03367065

Completed

Dynamic Contrast Enhancement Computed Tomography Based Techn...

Poitiers University Hospital Source

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Other study identifiers

Sponsor study identifier

PERFE-CT

Study Type

interventional

Actual enrollment (reported)

10

Locations

1 country

Sites

1

Timeline

Study Start

October 2016

Actual (reported)

Primary Completion

November 2017

Actual (reported)

Study Completion

December 2017

Actual (reported)

Brief Summary

This feasibility study has therefore several aims:

1.construct a dedicated CT perfusion protocol for GIT wall perfusion;
2.used a two-compartment pharmacokinetic model which is more adapted that a unique compartment model;
3.from the image acquired, evaluate current parameters of perfusion including the permeability ones

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 10 participants
Study completion date: December 2017
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
August 26, 2016
Actual (reported)
Study Start
October 2016
Actual (reported)
Primary Completion
November 2017
Actual (reported)
Study Completion
December 2017
Actual (reported)
First Posted
December 8, 2017
Actual (reported)

Last Updated: April 13, 2020
Status Verified: April 2020
Last Update Submitted: April 10, 2020

Conditions

Mesenteric Ischemia Permeability CT Technics

Outcome Measures

Primary Outcomes (1)

number of computerised tomography with interpretable data
2 hours

Study Arms (1)

Dynamic contrast enhanced computerised tomography

EXPERIMENTAL

Radiation: Dynamic contrast enhanced computerised tomography

Interventions

Dynamic contrast enhanced computerised tomographyRadiation

Dynamic contrast enhanced computerised tomography

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age50 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

all patients over fifty years old with clinico-biological suspicion for acute GITischemia admitted at our institution

You may not qualify if:

Sponsors & Collaborators

Poitiers University Hospital
Otherlead

Study Sites (1)

Chu Poitiers

Poitiers, Aquitaine, 86000, France

MeSH Terms

Conditions

Mesenteric Ischemia

Condition Hierarchy (Ancestors)

Intestinal DiseasesGastrointestinal DiseasesDigestive System DiseasesPeritoneal DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

Guillaume HERPE, MD
CHU Poitiers
PRINCIPAL INVESTIGATOR

Enrollment

10 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: DIAGNOSTIC
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

August 26, 2016

First Posted

December 8, 2017

Study Start

October 2016

Actual (reported)

NCT01389947

Microcirculation During Extracorporeal Circulation

Completed

NCT03484442

Multislice Computed Tomography Angiography in Acute Mesenteric Ischemia

Unknown

NCT05244629

Copenhagen Mesenteric Stent Study - A Randomized Trial of Stent Versus Covered Stent Treatment for Chronic Mesenteric Ischemia

Not ApplicableRecruiting

NCT02901808

Registeranalysis for the Examination of NOMI

Unknown

NCT03941015

Tissue Oxygenation During Treatment of Infant Congenital Heart Defects

Completed

NCT07059520

Translesional PRESSURE Measurements to Assess Clinical Relevance of a Mesenteric Artery Stenosis (PRESSURE-study)

Recruiting

contra-indication to contrast agent injection as so defined by the European Society of UroRadiology in 2014

inability to provide informed consent

Contact the study team to confirm eligibility.

Primary Completion

November 2017

Actual (reported)

Study Completion

December 2017

Actual (reported)

Last Updated

April 13, 2020

Record last verified: 2020-04

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT03367065
Data provider: ClinicalTrials.gov
Source updated: 2020-04-13
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:30:38 UTC

Locations

FR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

Primary Completion

Study Completion

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

Dynamic contrast enhanced computerised tomography

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations