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
| Type | Name | Description |
|---|---|---|
| DEVICE | Patient-regulated compression device | Compression of the abdomen with a patient-regulated compression device |
| DEVICE | Standard compression device | Compression 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.