Pre-operative Interventional Paramedical Consultation: What About the Implantable Device?

NCT ID
NCT07559981
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
University Hospital, Grenoble
Conditions
Anxiety, Paramedical Consultation

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 150 participants (Estimated).

What is being studied

  • Other: Paramedical consultation

Who may be eligible

Ages
18 Years to no maximum
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Patients scheduled to have an implantable port fitted in the Radiology Department at CHUGA * Patients aged 18 or over Exclusion Criteria: * Patients with a history of implantable port placement * Implantable port placement for a non-oncological indication * Emergency implantable port placement that could increase the patient's anxiety (port placement scheduled as an emergency within 7 days of the oncology consultation) * Subject currently excluded from another study * Persons referred to in Articles L1121-5 to L1121-8 of the Public Health Code (i.e. all protected persons: pregnant women, women in labour, breastfeeding mothers, persons deprived of their liberty by judicial or administrative order, and persons subject to a legal protection measure)

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: France

Sample of listed locations

  • University Hospital Grenoble — Grenoble, 38043, France — Recruiting

Study details

Start date
January 1, 2027
Primary completion date
January 1, 2030
Completion date
February 1, 2030
First posted
April 30, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07559981
Registry last updated
October 2, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07559981 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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