Nursing Clinical Trial
Official title:
Investigation of the Necessity of Aspiration During The Intramuscular Injection Administered in the Ventrogluteal Site and Its Effect on Pain
Verified date | June 2020 |
Source | Ege University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
H1: Aspiration is not necessary for IM injections applied from the ventrogluteal region.
H2: Aspiration procedure increases pain in IM injections applied from ventrogluteal region.
H3: The duration of the aspiration procedure on IM injections applied from the ventrogluteal
region is effective on pain.
Status | Active, not recruiting |
Enrollment | 834 |
Est. completion date | June 20, 2020 |
Est. primary completion date | June 10, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patient who came to the Emergency Service Care Unit for "Diclofenac Sodium" injection - Have no vision and hearing problems, - Who have no disease that may affect their perception of pain - Who can evaluate the "Visual Analog Scale" correctly, scoring 5 points or less from the VAS, - Body Mass Index is between 18.5-24.9 kg / m2, - Who do not have any discomfort in the extremities that will prevent them from taking the desired position, - No complications due to intramuscular injections such as abscess, infection, tissue necrosis and hematoma in the ventrogluteal region - No nodules or masses in the area Exclusion Criteria: - Patients who refuse the injection are excluded. |
Country | Name | City | State |
---|---|---|---|
Turkey | Ege University Hospital | Izmir |
Lead Sponsor | Collaborator |
---|---|
Ege University |
Turkey,
Beyea SC, Nicoll LH. Administration of medications via the intramuscular route: an integrative review of the literature and research-based protocol for the procedure. Appl Nurs Res. 1995 Feb;8(1):23-33. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Individual Introductory Information Form | The content of the study was explained to the patients coming to the emergency room. Written informed consents were obtained in line with the "Individual Introductory Information Form" of the patients. Individual Introductory Information Form: This form includes questions such as the patient's application group, diagnosis, age, gender, height, weight, and blood intake during aspiration in intramuscular injection. It is completed within the first 10-15 minutes of contact with the patient. |
15 minutes | |
Primary | Visual Analog Scale (VAS) | Intramuscular injection was performed in accordance with the application group assigned to the patients who filled the Individual Introductory Information Form. The patients were not told which group they belonged to. A nurse who except the researcher who performed the application evaluated pain levels that patients feel during injection immediately after the intramuscular injection application, with a Visual Analog Scale. The minimum score that can be obtained from this scale is 0 and the maximum score is 10. A higher score indicates that the pain is more severe. This scale was applied in minutes 1-5 after intramuscular injection. |
5 minutes |
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