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Effect of implementing local cooling in different times versus no implementation on pain severity and extend of bruise due to subcutaneous enoxaparin injection in cardiovascular patients

Effect of implementing local cooling in different times versus no implementation on pain severity and extend of bruise due to subcutaneous enoxaparin injection in cardiovascular patients: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201602029014N92
Enrollment
150
Registered
2016-02-11
Start date
2016-02-20
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

Pain. Pain, unspecified

Interventions

Intervention 1: ocal cooling using ice bag for 180 seconds 5 minutes before subcutaneous enoxaparin injection. Intervention 2: local cooling using ice bag for 180 seconds immediately after subcutaneou
Prevention
ocal cooling using ice bag for 180 seconds 5 minutes before subcutaneous enoxaparin injection
local cooling using ice bag for 180 seconds immediately after subcutaneous enoxaparin injection
Subcutaneous enoxaparin injection without any intervention

Sponsors

Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (a) age of 30 to 70 years; (b) indication of subcutaneous enoxaparin injection for the first time; (c) conscious and ability to percept and state the pain. Exclusion criteria: (a) receiving analgesic within past 4 hours; (b) death or discharge during 72 hours; (c) coagulopathy; (d) using anticoagulant agents.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Measuring pain severity. Timepoint: immediately after injection. Method of measurement: using visual analog scale.

Secondary

MeasureTime frame
Measuring extend of bruise. Timepoint: 12, 24, and 48 hours after injection. Method of measurement: using ruler.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMostafa Najafi

Farshchian Hospital

mostafanajafi115@gmail.com+98 81 3827 4184

Outcome results

None listed

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