Evaluation of Coronary Angiography

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 75

Inclusion Criteria

under non-emergency catheterization; age between 18-65 years; blood pressure less than 100/180 mmHg; the absence of active bleeding disorders; prothrombin time less than 16 seconds and time; Partial thromboplastin less than 90 seconds; no history of diabetes with disabilities; consent to participate in the study; angiography via the femoral artery; arterial puncture for the route only once; no DVT before the procedure; treatment with thrombolytic drugs and anticoagulant (taking warfarin); taking pain medication before the procedure; lack of peripheral vascular disease; no history of urinary problems; lack of sensitivity to contrast; no drug addiction; lack of chronic low back pain lack of blood and liver disease will be.
Exclusion criteria: active bleeding from the catheter entry with hemodynamic impairment and the need for blood transfusion; blood coagulation disorders; history of chronic low back pain; the need for cardiopulmonary resuscitation during angiography; chest pain with ECG changes; non-invasive blood pressure (NIBP) systolic or diastolic over and over mmHg 180 mmHg 100; disability and impaired level of consciousness in such a way that the patient is able to transform the work; rupture of the femoral artery during angiography; after a dangerous rhythm disorder Angiography; heparin injection during or after the procedure; the patient's hemodynamic status was while studying will be unhappy.

Exclusion Criteria

Not provided

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bleeding. Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: Measurement scales with a sensitivity of 0.1 g.;Hematoma. Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: with Trans Parente and graph paper.;Bruise. Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: with Trans Parente and graph paper.;Pain( include of back pain and groin pain). Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: NRS.;Urinary retention. Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: Based on asking from the patient.;Convenience. Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: VAS.;Thrombosis. Timepoint: at 0, 3, 6, 8 and 24 hours after angiography. Method of measurement: The sensory and motor symptoms, absence of peripheral pulse, the white appearance and painful physical examination.

Secondary Outcome Measures