Comparing Pain and Bruising of Subcutaneous Heparin Injection

NCT01645774 · Status: TERMINATED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2012-07-20

No results posted yet for this study

Summary

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.

Conditions

Interventions

PROCEDURE

10s injections duration

10s injections duration

PROCEDURE

10s injection duration and waiting 10s before withdrawing the needle

10s injection duration and waiting 10s before withdrawing the needle

PROCEDURE

15s injection duration and waiting 5s before withdrawing the needle

15s injection duration and waiting 5s before withdrawing the needle

PROCEDURE

5s injection duration and waiting 15s before withdrawing the needle

5s injection duration and waiting 15s before withdrawing the needle

Sponsors & Collaborators

  • Mashhad University of Medical Sciences

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
53 Years
Max Age
69 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2012-06-30
Completion
2012-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01645774 on ClinicalTrials.gov