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Recruiting NCT06776159

The Effect of Standardizing Procedures for SC Injections of LMWH on Patients With CVD

No phase Interventional CVD - Cardiovascular Disease Bruise Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Active Control, Standardized injection protocol.
Who it may be relevant to
Registry conditions: CVD - Cardiovascular Disease, Bruise, Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Hong Kong
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Standardizing Procedures for Subcutaneous Injections of Low-molecular-weight Heparin on Patients With Cardiovascular Diseases: A Cluster Randomized Controlled Trial

Overview

Improper subcutaneous administration of LMWH may cause complications at the injection site. Standardized protocol for subcutaneous LMWH injections in patient with cardiovascular diseases is warranted to ensure consistent best practices in clinical settings.

Detailed description

This study examines the effect of standardized protocol in reducing complications for patients with cardiovascular disease.

Interventions

  • Other Active Control
    Patients in the control group will receive the usual practice of subcutaneous LMWH injection administered by nurses.
  • Other Standardized injection protocol
    Nurses administer LMWH according to the standardized evidence-based protocol.

Primary outcome measures

  • Bruising [Time frame: 24 hours, 48 hours, 72 hours]
  • Pain [Time frame: Immediately after injection, 24 hours, 48 hours, 72 hours]
Secondary outcome measures (2)
  • Patient Experience [Time frame: Immediately after receiving the injection]
  • Communicative Competence [Time frame: Immediately before and after injection]

Eligibility criteria

Inclusion criteria

  • patients who are in cardiac care units suffering from cardiovascular diseases prescribed with LMWH injections two times per day
  • Chinese

Exclusion criteria

  • cognitively impaired
  • unconscious
  • refuse to participate

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Hong Kong · 1 center
  • Hospital Authority, Hong Kong — Hong Kong

Identifiers

NCT: NCT06776159 · 20250301 · CHEUNGPuiYu

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗