- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01645774
Comparing Pain and Bruising of Subcutaneous Heparin Injection
Subcutaneous heparin injection is one of the most frequent nurses' clinical care. This study aimed to Identify and compare the effects of four different injection duration on pain and bruising associated with subcutaneous injection of heparin in 90 patients. Four injection methods were used for them:
A: 10s injections duration
B: 10s injection duration and waiting 10s before withdrawing the needle
C: 15s injection duration and waiting 5s before withdrawing the needle
D: 5s injection duration and waiting 15s before withdrawing the needle.
Bruising was measured by a flexible millimeter ruler 48h after each injection; and pain was measured by pain visual analogue scale immediately after the injection. Data will be analyzed by SPSS.
Study Overview
Status
Study Type
Enrollment (Actual)
Phase
- Phase 2
- Phase 3
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Inclination to participate in the study; filling out the form of conscious satisfaction
- Ability to answer the questions and determining the rate of pain
- Not being affected by blood clotting difficulties, tissue damages, injuries, and bruises in the site of injection.
Exclusion Criteria:
- Death,
- Discharge
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: 10s injections duration
|
10s injections duration
|
Experimental: 10s injection duration , waiting 10s
10s injection duration and waiting 10s before withdrawing the needle
|
10s injection duration and waiting 10s before withdrawing the needle
|
Experimental: 15s injection duration,waiting 5s
15s injection duration and waiting 5s before withdrawing the needle
|
15s injection duration and waiting 5s before withdrawing the needle
|
Experimental: 5s injection duration , waiting 15s
5s injection duration and waiting 15s before withdrawing the needle
|
5s injection duration and waiting 15s before withdrawing the needle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
decrease pain
Time Frame: up to 6 months
|
pain was measured by pain visual analogue scale immediately after the injection.
|
up to 6 months
|
bruising
Time Frame: up to 6 months
|
Bruising was measured by a flexible millimeter ruler 48h after each injection
|
up to 6 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Wounds and Injuries
- Wounds, Nonpenetrating
- Contusions
- Physiological Effects of Drugs
- Adrenergic Agents
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Autonomic Agents
- Peripheral Nervous System Agents
- Adrenergic alpha-Agonists
- Adrenergic Agonists
- Respiratory System Agents
- Sympathomimetics
- Vasoconstrictor Agents
- Nasal Decongestants
- Oxymetazoline
Other Study ID Numbers
- Interventional (Oncolys BioPharma Inc)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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