Health Condition 1: null- Reduction in phlebitis and pain within 24hours using magnesium sulphate paste application.
Conditions
Interventions
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: -Patients who developed phlebitis only in the upper limb with visual infusion phlebitis score of two or more. -Patients who are 18 to 65 years old. -Patients with infusion-related phlebitis and not received any form of intervention by a staff nurse. -Patients who can speak Tamil, English, Hindi, and Telugu.
Exclusion criteria
Exclusion criteria: -Patients who are allergic to Glycerine Magnesium Sulphate paste or heparinoid (thrombophob) ointment. -Patients on central venous catheter on the same side of the limb, dermatological disorder, cardiac problems, lymphatic obstruction, Haematological disorders and bleeding disorders -Patients on intravenous chemotherapy. -Patients with injury on the same side of the limb.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare the effectiveness of Glycerine Magnesium Sulphate paste and heparinoid (thrombophob) ointment by assessing the reduction in phlebitis and pain intensity at every 24 hours on patients with peripheral intravenous therapy.Timepoint: The investigator will assess the participantâ??s phlebitis condition and grade it using Visual Infusion Phlebitis Scale (VIP) as (1,2,3,4,5)and will also assess the pain level using Numerical pain rating scale( No pain; 0, Mild pain :1-3, Moderate pain:4-6, Severe pain : 7-10), pre intervention and post intervention at 24 hours and at 48 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine association between the effectiveness of Glycerine Magnesium sulphate paste with selected demographic and clinical variable. To determine association between the effectiveness of heparinoid (thrombophob) ointment with selected demographic and clinical variable.Timepoint: The investigator will assess the participantâ??s phlebitis condition and grade it using Visual Infusion Phlebitis Scale (VIP) as (1,2,3,4,5)and will also assess the pain level using Numerical pain rating scale( No pain; 0, Mild pain :1-3, Moderate pain:4-6, Severe pain : 7-10), pre intervention and post intervention at 24 hours and at 48 hours. | — |
Countries
India
Contacts
College of Nursing, Christian Medical College, Vellore, Tamil Nadu, India.