Clinical Trials Directory

Trials / Completed

CompletedNCT02622269

Patient-driven Compression in Urography

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Örebro University, Sweden · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Compression of the abdomen during urography with either a patient-regulated compression device or conventional compression. Evaluation of radiation dose, image quality and patients' experiences

Detailed description

Patients are subjected to radiation from radiographical studies. The nurse can reduce the radiation dose for the individual by using dose-reducing measures. One of these is compression. It is known that compression in urography reduces the radiation dose because the radiation has less tissue to transverse when it is compressed. By reducing patient radiation doses, the risk of harmful radiation effects is reduced. This study aims to study if a patient-regulated compression device can reduce the radiation dose as effectively as the conventional compression, regulated by the nurse. Two compression devices are investigated in each patient, in randomized order. Aims of the study: 1. Evaluate if the radiation doses are comparable with a patient-regulated compression device and conventional compression. 2. Evaluate image quality with the two devices. 3. Describe patients' experiences from using the two devices.

Conditions

Interventions

TypeNameDescription
DEVICEPatient-regulated compression deviceCompression of the abdomen with a patient-regulated compression device
DEVICEStandard compression deviceCompression of the abdomen with the standard compression device

Timeline

Start date
2015-04-01
Primary completion
2016-01-01
Completion
2016-01-01
First posted
2015-12-04
Last updated
2016-02-25

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT02622269. Inclusion in this directory is not an endorsement.