Study of Whether 15 mg Dose of Ketorolac IV is as Effective as a 30 mg Dose.
Primary Purpose
Pain, Pain, Postoperative
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Ketorolac Tromethamine
Ketorolac Tromethamine
Sponsored by
About this trial
This is an interventional treatment trial for Pain focused on measuring Pain, Postoperative, Ketorolac, Anti-Inflammatory Agents, Non-Steroidal, Intraoperative Care
Eligibility Criteria
Inclusion Criteria:
- Patients booked for 1-2 level spine laminectomies and/or decompression
- Adult 18 - 65 years
- Weight of 50 - 110 kg
Exclusion Criteria:
- Previous lumbar laminectomy
- Current anticoagulant use with INR > 1.2
- Narcotic use > 4 weeks
- Known allergy or sensitivity to NSAID or morphine
- Renal insufficiency with creatinine >100 umol/L
- Known liver disease
- History of gastrointestinal bleeding
- Pregnancy, history of bronchial asthma
- NSAID use 2 days before surgery.
Sites / Locations
- Foothills Medical CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
15 mg ketorolac IV
30 mg ketorolac IV
Arm Description
Outcomes
Primary Outcome Measures
Visual Analog Score
To show the non-inferiority of 15 mg intraoperative dose of ketorolac as compared to the standard 30 mg ketorolac by looking at the VAS scores 4 hours after an adult spine surgery. Minimum clinically significant decrease in VAS pain score is 18 mm.
Secondary Outcome Measures
Morphine Usage After Surgery
A 10 mg decrease in morphine use in 24 hours is considered clinically significant.
Morphine Adverse Effects
Presence of morphine-related adverse effects such as sedation, nausea, vomiting, respiratory depression, and pruritus.
Postoperative Bleeding
Hemoglobin levels will be measured before surgery and 24 hours surgery.
Full Information
NCT ID
NCT01230463
First Posted
October 27, 2010
Last Updated
October 27, 2010
Sponsor
University of Calgary
1. Study Identification
Unique Protocol Identification Number
NCT01230463
Brief Title
Study of Whether 15 mg Dose of Ketorolac IV is as Effective as a 30 mg Dose.
Official Title
Intraoperative Ketorolac Dose of 15 mg Versus the Standard 30 mg on Early Postoperative Pain After Spine Surgery: A Randomised, Blinded, Non-Inferiority Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2010
Overall Recruitment Status
Unknown status
Study Start Date
September 2010 (undefined)
Primary Completion Date
September 2011 (Anticipated)
Study Completion Date
September 2011 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
University of Calgary
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary aim of this study is to show the non-inferiority of 15 mg intraoperative dose of ketorolac as compared to the standard 30 mg ketorolac by looking at the VAS scores 4 hours after an adult spine surgery.
Detailed Description
Opioids have traditionally been the cornerstone of acute postoperative pain management. Problematic side effects such as nausea, vomiting, ileus, urinary retention, excess sedation, and respiratory depression are significant disadvantages with the use of opioids. Alternative treatments have been sought. The concept of adding a nonsedating non opioid analgesic agent is appealing and has been validated by previous studies. Nonsteroidal anti-inflammatory drugs (NSAID) are nonsedating and combine analgesic and anti-inflammatory properties ideal for pain after surgery.
Ketorolac is a potent intravenous nonsteroidal anti-inflammatory drug (NSAID), and a non selective cyclooxygenase inhibitor which mediates pain, inflammation and fever. It has been evaluated and used for treatment of moderate to severe pain including postoperative pain. Although intravenous route is not approved by Health Canada, its use is supported in medical literature and clinical practice.
Previous studies have demonstrated the effectiveness of standard 30 mg intravenous ketorolac as an adjunct to opioids for postoperative pain relief. Standard parenteral dose recommended by manufacturer for healthy non elderly population is 30 mg based on a number clinical trials.
Alberta Health Services (AHS) Pharmacy formulary has approved the intravenous use of ketorolac in the dosage range of 10-30 mg depending the patient's weight and medical comorbidities.
NSAIDs, including ketorolac, have an analgesic ceiling effect in which higher doses do not provide any additional pain relief but may increase the likelihood of side effects. Single dose IM ketorolac have been studied in the past showing no difference in analgesia with the 30 and 90 mg dose. Because of risk of drug toxicity and unwanted side effects, patients should be given the lowest effective ketorolac dose. Low dose ketorolac was studied in the adolescents undergoing spine surgery and showed that dose of 0.2mg/kg (11mg) provides supplemental analgesia postoperatively. However, there were no previous studies found on review of the literature using medline search that look at parallel comparison between intraoperative doses of ketorolac in terms of efficacy and safety profile.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Pain, Postoperative
Keywords
Pain, Postoperative, Ketorolac, Anti-Inflammatory Agents, Non-Steroidal, Intraoperative Care
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
15 mg ketorolac IV
Arm Type
Active Comparator
Arm Title
30 mg ketorolac IV
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Ketorolac Tromethamine
Other Intervention Name(s)
Toradol
Intervention Description
15 mg ketorolac IV as a bolus 30 minutes before closure of surgery.
Intervention Type
Drug
Intervention Name(s)
Ketorolac Tromethamine
Other Intervention Name(s)
Toradol
Intervention Description
30 mg ketorolac IV as a bolus 30 minutes before closure of surgery.
Primary Outcome Measure Information:
Title
Visual Analog Score
Description
To show the non-inferiority of 15 mg intraoperative dose of ketorolac as compared to the standard 30 mg ketorolac by looking at the VAS scores 4 hours after an adult spine surgery. Minimum clinically significant decrease in VAS pain score is 18 mm.
Time Frame
Four hours after surgery
Secondary Outcome Measure Information:
Title
Morphine Usage After Surgery
Description
A 10 mg decrease in morphine use in 24 hours is considered clinically significant.
Time Frame
8 hours and 24 hours after surgery
Title
Morphine Adverse Effects
Description
Presence of morphine-related adverse effects such as sedation, nausea, vomiting, respiratory depression, and pruritus.
Time Frame
First 24 hours
Title
Postoperative Bleeding
Description
Hemoglobin levels will be measured before surgery and 24 hours surgery.
Time Frame
24 hours after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients booked for 1-2 level spine laminectomies and/or decompression
Adult 18 - 65 years
Weight of 50 - 110 kg
Exclusion Criteria:
Previous lumbar laminectomy
Current anticoagulant use with INR > 1.2
Narcotic use > 4 weeks
Known allergy or sensitivity to NSAID or morphine
Renal insufficiency with creatinine >100 umol/L
Known liver disease
History of gastrointestinal bleeding
Pregnancy, history of bronchial asthma
NSAID use 2 days before surgery.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cecilia Deguzman, MD
Phone
403-944-1991
Email
Cecilia.DeGuzman@albertahealthservices.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Kevin Yee, MD
Phone
403-944-1991
Email
kevin.yee@albertahealthservices.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kaylene Duttchen, MD
Organizational Affiliation
University of Calgary - Department of Anesthesia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Melinda Davis, MD
Organizational Affiliation
University of Calgary - Department of Anesthesia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Foothills Medical Centre
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 2T9
Country
Canada
Individual Site Status
Recruiting
12. IPD Sharing Statement
Learn more about this trial
Study of Whether 15 mg Dose of Ketorolac IV is as Effective as a 30 mg Dose.
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