Acute Pain Clinical Trial
Official title:
Comparison of Ketamine 0.1 mg/kg, 0.2 mg/kg, and 0.3 mg/kg Intravenous Doses for Acute Pain in the Emergency Department: A Prospective, Randomized, Double-blind, Active-controlled, Clinical Trial
Verified date | May 2023 |
Source | Hackensack Meridian Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will prospectively compare the mean Numerical Rating Scale (NRS) pain score reduction amongst three recommended dosing strategies of intravenous ketamine (0.1 mg/kg, 0.2 mg/kg, and 0.3mg/kg) for acute pain in the emergency department (ED).This study will also examine the frequency of adverse events secondary to ketamine including fatigue, dizziness, nausea, headache, feeling of unreality, changes in hearing or vision, mood changes, generalized discomfort, and hallucinations, changes in vital signs. Subgroups for exploratory analysis based on the need for rescue analgesia within two hours of ketamine administration, adequate pain relief, previous opioid tolerance, and age (adults < 65 years old and > 65 years old).
Status | Terminated |
Enrollment | 11 |
Est. completion date | December 20, 2019 |
Est. primary completion date | December 20, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility | Inclusion Criteria: - Acute pain (including acute on chronic pain) - Pain score of moderate to severe (> 4/10) on the Numerical Rating Scale - Provider determines the patient requires intravenous ketamine for analgesia Exclusion Criteria: - History of hypersensitivity to ketamine - Altered mental status - Psychiatric illness - Known history of renal or hepatic insufficiency - Acute head or eye injury - Suspected intracranial hypertension or mass - Headache as the chief complaint - Alcohol or drug abuse - Received an analgesic within the last four hours - History of congestive heart failure - History of aortic or brain aneurysm - Active Chest Pain - Porphyria - Active methadone treatment - Pregnant or breastfeeding - Signs of respiratory, hemodynamic, or neurologic compromise - Systolic blood pressure < 90 mmHg or > 180 mmHg - Heart rate < 50 beats per minute or > 150 beats per minute - Respiratory rate < 10 breaths per minute or > 30 breaths per minute - Glasgow Coma Score < 15 - Previously received ketamine < 0.3 mg/kg IV for acute pain in the emergency department |
Country | Name | City | State |
---|---|---|---|
United States | Hackensack University Medical Center | Hackensack | New Jersey |
Lead Sponsor | Collaborator |
---|---|
Hackensack Meridian Health |
United States,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain Score | Pain score using Numerical Rating Scale (NRS) post ketamine infusion. The Numerical Rating Scale (NRS) ranges from 0-to-10 with 0 being no pain and lower numbers representing less pain, so in this case lower numbers will represent better outcomes.
Pain scores were reported at baseline and then at 15 min/30 min/60 min/90 min and 120 minutes post-infusion. |
Within 2 hours post infusion completion | |
Secondary | Adverse Events | Frequency of adverse events secondary to ketamine including fatigue, dizziness, nausea, headache, feeling of unreality, changes in hearing or vision, mood changes, generalized discomfort, and hallucinations, changes in vital signs.
Adverse events were reported at baseline and then at 15 min/30 min/60 min/90 min and 120 minutes post-infusion. |
Within 2 hours post infusion completion |
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