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Evaluation of Coronary Angiography

The Comparative Study of the Effects of Sand Bag Keeping Time and Changing Body Position on Acute Complications of Coronary Angiography.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015091424018N1
Enrollment
75
Registered
2015-11-14
Start date
2015-10-07
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

complication of cronary angiography. Atherosclerosis of other arteries( coronary arteries)

Interventions

Intervention 1: control group: patients in the control group, will receive routines care include of 8 hours motionless in supine position, with head angle of zero degrees, rest in bed and preserving
Prevention
control group: patients in the control group, will receive routines care include of 8 hours motionless in supine position, with head angle of zero degrees, rest in bed and preserving a 4 kg sandbag
sandbag’s intervention group: patients in sandbag’s intervention group will receive routines care except that in the third hour after entering to the heart ward, sandbag will be removed from the pos
Changing body Position’s intervention group: patients in Changing body Position’s intervention group will receive routines care except that the following positions during bed rest will be applied. D

Sponsors

Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSina Valiee

Kurdistan University of Medical Sciences

sinavaliee@yahoo.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026