Injection Site Irritation
Conditions
Keywords
dexketoprofen, pain, rocuronium
Brief summary
Purpose : The aim of the study is to investigate the effects of cox inhibitors as a rescue agent against the rocuronium pain Methodology : Sixty patients enrolled for the general anesthesia enrolled in this study. Patients were allocated into two groups (Group 1: Dexketoprofen group, Group 2: Control group) .Pain was evaluated by during rocuronium injection, patients were scored by a scale showed below. 0;No movement response to injection 1. Mild movement response to injection 2. Hand withdrawal response to injection 3. Arm withdrawal response to injection Investigators also evaluated the pain with 2 questions when the patient was in the recovery room. Question 1.What was the last feeling before participants fall into sleep? question 2. Did participants feel any pain on participants's hand during medication injection for anesthesia?
Detailed description
Purpose : Rocuronium bromide is a painful agent while general anesthesia induction. The aim of the study is to investigate the effects of cox inhibitors as a rescue agent against the rocuronium pain Methodology : Sixty patients enrolled for the general anesthesia enrolled in this study. Patients were allocated into two groups (Group 1: Dexketoprofen group, Group 2: Control group) .Pain was evaluated by during rocuronium injection, patients were scored by a scale showed below. 0;No movement response to injection 1. Mild movement response to injection 2. Hand withdrawal response to injection 3. Arm withdrawal response to injection Investigators also evaluated the pain with 2 questions when the patient was in the recovery room. Question 1.What was the last feeling before participants fall into sleep? question 2. Did participants feel any pain on participants's hand during medication injection for anesthesia?
Interventions
intravenous dexketoprofen (KETAVEL 50 mg/2 ml)
DRUGSaline (Isotonic Saline Solution 0.9% )
intravenous 2 ml of saline
Sponsors
Ankara City Hospital Bilkent
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* non allergic to dexketoprofen * 18-60 years old * American Society of Anesthesiologists(ASA) 1-2-3 * 70-90 kg weigh
Exclusion criteria
* patients with psychiatric and mental problems
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The injection pain due to rocuronium | 1 month | Pain will be recorded and graded using a 4-point scale (none, mild, moderate, or severe). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Score on pain due to injection of rocuronium | 1 month | Withdrawal reactions are scored as follows: (a) no pain response, (b)pain limited to the wrist, (c) pain limited to the elbow/shoulder, or (d) generalized pain response. |
Countries
Turkey (Türkiye)
Outcome results
None listed