Intranasal Ketamine Versus Subcutaneous Ketamine for Treatment of Post-traumatic Acute Pain in the Emergency Department ( INVESCK )
Acute Pain
About this trial
This is an interventional treatment trial for Acute Pain
Eligibility Criteria
Inclusion Criteria:
• Patients who presented to the ED with acute limb trauma pain with a visual analgesic scale (VAS) of 5 or more on a standard 11 point (0-10).
- Pain was considered traumatic if it is reported as appearing immediately after the trauma and no anterior pain was described in the same limb.
Exclusion Criteria:
Pregnancy/Breastfeeding
- altered mental status (GCS<15)
- Allergy to ketamine or morphine
- Weight less than 40 kg or greater than 100kg
- Unstable vital signs (systolic blood pressure <90 or > 180mmHg, pulse rate<50 or >150bpm, and respiration rate <10 or >30 breath/min)
- Medical history of acute head or eye injury
- Medical history of seizure
- Medical history of intracranial hypertension,
- Medical history of chronic pain,
- Medical history of severe renal or hepatic insufficiency.
- Medical history of glaucoma
- Alcohol or drug abuse
- Psychiatric illness,
- Recent (4 hours before) analgesic agent use.
Sites / Locations
- university of MonastirRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Intranasal ketamine
subcutanous ketamine
Ketamine solution 250 mg/5ml was used. It was applied intranasally using a nasal spray pump whereeach spray delivered approximately 0.4 ml of solution corresponding to 20 mg of ketamine. After initial evaluation, each patient having the inclusion criteria receives one pulverisation (0.4 ml) per nostril of ketamine corresponding to a total dose of 20 mg of ketamine. Ketamine dosing was based on previous reports of intranasal ketamine use in ED patients, doses ranged from 0.45mg/kg to 1.25mg/kg (9).
Ketamine dosing by subcutanous route was based on previous reports use for post operative pain management. . The results of these reports revealed that low-dose ketamine 20-60 mg (0.5mg/kg for patients weighing 40-120 kg) showed an over all decrease in either the amount of opioid used or the amount of pain experienced (10, 11).For our study, we decided to chose a dose of 20mg of ketamine for all patients administered via 1ml insulin syringe once subcutaneously.