Skip to content

Comparison of sand bag and closure pad on the reducing bleeding and hematoma

Comparison the influence of sand bag and closure pad on vascular complication of patients undergoing Angiography and admitted at Imam Ali Hospital (2015)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201404134736N5
Enrollment
250
Registered
2015-08-19
Start date
2015-08-23
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

Coronary Artery Diseases. Atherosclerotic heart disease Coronary (artery): • atheroma • atherosclerosis • disease • sclerosis

Interventions

Intervention 1: Intervention 1: closure pad will be used. In this group amount of bleeding will be measured immediately and every half an hour for 24 hours and hematoma size will be measured immediat
Prevention
Intervention 1: closure pad will be used. In this group amount of bleeding will be measured immediately and every half an hour for 24 hours and hematoma size will be measured immediately and every 6
Intervention 2: Sand bag will be used. In this group amount of bleeding will be measured immediately and every half an hour for 24 hours and hematoma size will be measured immediately and every 6 ho

Sponsors

Vice chancellor for research, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: non-emergency angiography, full consciousness, the use of the right femoral artery for vascular access, age between 18-80 years, the use of sheath No. 6 (fr), the absence of pregnancy and lactation in females, absence of disorder bleeding disorder such as hemophilia, lack of infection of the groin, no peripheral arterial diseases such as Raynaud's, normal blood pressure, normal blood coagulation tests (PT, PTT, INR), not receiving anticoagulant and glomerular filtration rate above 50mg/dl respectively. Exclusion criteria: the primary hemostasis more than 30 minutes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Amount of bleeding. Timepoint: Immediately after angiography and every half an hour up to 24 hours. Method of measurement: Weighing gases of angiography site.;Hematoma size. Timepoint: Immediately after angiography and every 6 hours up to 24 hours. Method of measurement: Checkered ruler.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Khatony

Kermanshah University of Medical Sciences

akhatony@gmail.com+98 83 3828 2102

Outcome results

None listed

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