Clinical Trials Directory

Trials / Completed

CompletedNCT00259194

Observation and Prediction of Complications After Coronary Angiography

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,000 (estimated)
Sponsor
Herning Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Coronary angiography via the femoral artery is regarded as a safe procedure, but bleeding complications are often seen. To avoid/reduce bleeding complications digital compression is applied in the area of puncture during approximately 20 minutes and the patient is in the investigators' department observed in bed for 2 hours. The investigators apply pressure over the puncture site using a sand bag in the first hour. The patients are told not to move, to keep their legs and upper arms down and not to lift the head from the pillow in these 2 hours (standard observation). In the present study the patients are randomized between standard observation and an alternative observation, where the patients are allowed to lift their head, arms and legs during the 2 hours, otherwise as standard observation. The study has three aims: 1. To establish the incidence of bleeding complications: * Frequency of hematoma (\> 5 cm) * Frequency of pseudoaneurysms * Frequency of bleeding demanding surgery * Frequency of bleeding demanding transfusion 2. Establish a model to predict in wich patient to expect a bleeding complication. 3. Assess if the alternative observation is associated with more bleeding complications compared to standard observation.

Conditions

Interventions

TypeNameDescription
BEHAVIORALMovingThe patients are allowed to lift their head, arms and legs during the 2 hours.
BEHAVIORALNo MovingThe patients are told not to move, to keep their legs and upper arms down and not to lift the head from the pillow in these 2 hours.

Timeline

Start date
2005-12-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2005-11-29
Last updated
2009-06-11

Locations

2 sites across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00259194. Inclusion in this directory is not an endorsement.