Effect of Changing weight of sand bag on some complications of coronary angiography

Phase 2

• Conditions: cardiac catheterization.

• Registration Number: IRCT2013052213424N1
• Lead Sponsor: Vice chancellor for research, Golestan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 140

Inclusion Criteria

non-emergency catheterization of the femoral artery and catheter 6fr build a company; withdrawal of arterial sheath immediately after angiography; aged 18-65; systolic blood pressure less than 180 and a diastolic pressure of less than 100; the lack of bleeding disorders Off; Pt <16, ptt <50, INR <1/8; the absence of peripheral vascular disease; no history of previous low back pain; lack of experience difficulty passing urine; loss of cerebrovascular accidents and motor and neuromuscular problems; lack of angioseal, BMI 18/5-29; informed consent to participate in the study.
Exclusion criteria: the need for angiography during cardiopulmonary resuscitation; chest pain with new ECG changes; hemodynamic changes associated with active bleeding and need for blood transfusion; dangerous arrhythmias immediately after cardiac catheterization; vascular injury during the procedure; hemostasis time after the procedure; a long (over 20 minutes); use of pain medications; heparin infusion during or after catheterization; manipulating both the femoral artery and arterial catheter in place for more than 2 times; patient unwillingness to participate in the study.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bleeding. Timepoint: On arrival the patient, every 2 hours for 8 hours and then 24 hours later. Method of measurement: Christenson check list.;Hematoma. Timepoint: On arrival the patient, every 2 hours for 8 hours and then 24 hours later. Method of measurement: Christenson check list.;Pain. Timepoint: On arrival the patient, every 2 hours for 8 hours and then 24 hours later. Method of measurement: Numeric pain scale.;Urinary retention. Timepoint: On arrival the patient, every 2 hours for 8 hours and then 24 hours later. Method of measurement: Question of patient.;Comfort. Timepoint: On arrival the patient, every 2 hours for 8 hours and then 24 hours later. Method of measurement: Visual scale Comfort.

Secondary Outcome Measures

Name	Time	Method
Protromobin time (PT). Timepoint: Before intervention. Method of measurement: second.