search
Back to results

IM Ketorolac vs Cambia for the Acute Treatment of Severe Migraine

Primary Purpose

Migraine Headache

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Diclofenac postassium powder for oral solution and placebo injection
Ketorolac intramuscular injection and placebo oral solution
Sponsored by
Scripps Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Migraine Headache focused on measuring Severe Migraine Headache

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who meet IHS criteria for migraine
  • Age 18 to 65
  • At least 2 migraine attacks per month
  • Able to give written consent
  • Willing to complete the entire course of the study
  • Current headache duration greater than or equal to 36 hours

Exclusion Criteria:

  • Pregnant or nursing
  • Significant medical or psychiatric disease
  • History of gastritis, gastric ulcer, GI bleed
  • Renal insufficiency
  • Hepatic insufficiency
  • History of opioid dependence within the last 10 years or currently
  • Any current or prior use of DICLOFENAC POTASSIUM POWDER FOR ORAL SOLUTION (CAMBIA)
  • Past allergic reaction to DICLOFENAC or other NSAIDs

Sites / Locations

  • Scripps ClinicRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Cambia

ketorolac

Arm Description

Diclofenac postassium powder for oral solution and placebo injection

ketorolac intramuscular injection and placebo oral solution

Outcomes

Primary Outcome Measures

Pain relief, 0-3 scale
Pain free response, 0-3 scale
Sustained pain free response, 0-3 scale

Secondary Outcome Measures

Change in severity of migraine associated symptoms
Disability, Nausea, Photophonia/phonophobia self reported using a 0-3 rating scale
Return to function
Severity, Disability, Nausea, Photophonia/phonophobia self reported as 0 on 0-3 scale

Full Information

First Posted
January 18, 2016
Last Updated
February 1, 2016
Sponsor
Scripps Health
Collaborators
Depomed
search

1. Study Identification

Unique Protocol Identification Number
NCT02664116
Brief Title
IM Ketorolac vs Cambia for the Acute Treatment of Severe Migraine
Official Title
IM Ketorolac vs Diclofenac Potassium Powder for Oral Solution (Cambia) for the Acute Treatment of Severe Migraine
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
July 2017 (Anticipated)
Study Completion Date
July 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Scripps Health
Collaborators
Depomed

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This research will be conducted to see if the oral drug Cambia is as effective in relieving severe migraine headaches as the injectable drug ketorolac.
Detailed Description
The treatment of severe migraine often requires a patient office visit or treatment in the ER or urgent care setting. This is due to the minimal efficacy of PO treatments once migraine is severe, and therefore the need for parenteral treatments. IM Ketorolac is one mainstay of parenteral treatment. There is an unmet need for effective at-home treatment regimens for severe migraine. Despite FDA approval of Cambia for acute migraine treatment, insurance is reticent to cover the treatment due to higher cost in comparison to generic diclofenac tablets, despite superior efficacy of Cambia in comparison to generic diclofenac tablets (Diener, Cephalalgia 2006). One objective of this study would be to provide rationale to justify the insurance coverage of this treatment in comparison to generic tablets, because at home treatment is less costly than office visit or emergency department visit to receive IM ketorolac. A previous study of Cambia demonstrated that this formulation of diclofenac potassium for oral solution is effective in reducing pain intensity within 30 minutes, which may be related to the 15-minute Tmax associated with this formulation. The rapid-onset benefits were sustained through 24 hours post-treatment (Lipton, Cephalalgia 2010)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine Headache
Keywords
Severe Migraine Headache

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cambia
Arm Type
Experimental
Arm Description
Diclofenac postassium powder for oral solution and placebo injection
Arm Title
ketorolac
Arm Type
Active Comparator
Arm Description
ketorolac intramuscular injection and placebo oral solution
Intervention Type
Drug
Intervention Name(s)
Diclofenac postassium powder for oral solution and placebo injection
Other Intervention Name(s)
Cambia
Intervention Description
Diclofenac postassium powder for oral solution 50 mg in 1 ounce water orally, single dose and placebo normal saline 2ml intramuscular injection, single dose
Intervention Type
Drug
Intervention Name(s)
Ketorolac intramuscular injection and placebo oral solution
Other Intervention Name(s)
Toradol
Intervention Description
ketorolac 60 mg in 2 ml intramuscular injection, single dose and placebo oral solution, 1 ounce, single dose
Primary Outcome Measure Information:
Title
Pain relief, 0-3 scale
Time Frame
Change from baseline pain rating at 5, 10, 15, 30, and 60 minutes post intervention
Title
Pain free response, 0-3 scale
Time Frame
2 hours post intervention
Title
Sustained pain free response, 0-3 scale
Time Frame
24 hours post intervention
Secondary Outcome Measure Information:
Title
Change in severity of migraine associated symptoms
Description
Disability, Nausea, Photophonia/phonophobia self reported using a 0-3 rating scale
Time Frame
5, 10, 15, 30, 60, 120 minutes and 24 hours post intervention
Title
Return to function
Description
Severity, Disability, Nausea, Photophonia/phonophobia self reported as 0 on 0-3 scale
Time Frame
24 hours post intervention

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 who meet IHS criteria for migraine Age 18 to 65 At least 2 migraine attacks per month Able to give written consent Willing to complete the entire course of the study Current headache duration greater than or equal to 36 hours Exclusion Criteria: Pregnant or nursing Significant medical or psychiatric disease History of gastritis, gastric ulcer, GI bleed Renal insufficiency Hepatic insufficiency History of opioid dependence within the last 10 years or currently Any current or prior use of DICLOFENAC POTASSIUM POWDER FOR ORAL SOLUTION (CAMBIA) Past allergic reaction to DICLOFENAC or other NSAIDs
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emily Rubenstein Engel, MD
Phone
858-554-8887
Email
Engel.EmilyRubenstein@scrippshealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily Rubenstein Engel, MD
Organizational Affiliation
Scripps Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Scripps Clinic
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emily Rubenstein Engel, M.D.
Phone
858-554-8887
Email
Engel.EmilyRubenstein@scrippshealth.org

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual Patient Data will not be made available
Citations:
PubMed Identifier
25288700
Citation
Factor SA, Jankovic J. Randomized trial of IV valproate vs metoclopramide vs ketorolac for acute migraine. Neurology. 2014 Oct 7;83(15):1388-9. doi: 10.1212/01.wnl.0000455698.16732.0a. No abstract available.
Results Reference
background
PubMed Identifier
25034250
Citation
Garnock-Jones KP. Diclofenac potassium powder for oral solution: a review of its use in patients with acute migraine. CNS Drugs. 2014 Aug;28(8):761-8. doi: 10.1007/s40263-014-0186-y.
Results Reference
background
PubMed Identifier
24523483
Citation
Friedman BW, Garber L, Yoon A, Solorzano C, Wollowitz A, Esses D, Bijur PE, Gallagher EJ. Randomized trial of IV valproate vs metoclopramide vs ketorolac for acute migraine. Neurology. 2014 Mar 18;82(11):976-83. doi: 10.1212/WNL.0000000000000223. Epub 2014 Feb 12.
Results Reference
background
PubMed Identifier
23298250
Citation
Taggart E, Doran S, Kokotillo A, Campbell S, Villa-Roel C, Rowe BH. Ketorolac in the treatment of acute migraine: a systematic review. Headache. 2013 Feb;53(2):277-87. doi: 10.1111/head.12009. Epub 2013 Jan 8.
Results Reference
background
PubMed Identifier
20959428
Citation
Lipton RB, Grosberg B, Singer RP, Pearlman SH, Sorrentino JV, Quiring JN, Saper JR. Efficacy and tolerability of a new powdered formulation of diclofenac potassium for oral solution for the acute treatment of migraine: results from the International Migraine Pain Assessment Clinical Trial (IMPACT). Cephalalgia. 2010 Nov;30(11):1336-45. doi: 10.1177/0333102410367523. Epub 2010 Apr 7.
Results Reference
background
PubMed Identifier
1514724
Citation
Duarte C, Dunaway F, Turner L, Aldag J, Frederick R. Ketorolac versus meperidine and hydroxyzine in the treatment of acute migraine headache: a randomized, prospective, double-blind trial. Ann Emerg Med. 1992 Sep;21(9):1116-21. doi: 10.1016/s0196-0644(05)80654-7.
Results Reference
background
PubMed Identifier
24875925
Citation
Orr SL, Aube M, Becker WJ, Davenport WJ, Dilli E, Dodick D, Giammarco R, Gladstone J, Leroux E, Pim H, Dickinson G, Christie SN. Canadian Headache Society systematic review and recommendations on the treatment of migraine pain in emergency settings. Cephalalgia. 2015 Mar;35(3):271-84. doi: 10.1177/0333102414535997. Epub 2014 May 29.
Results Reference
background
PubMed Identifier
25600718
Citation
Marmura MJ, Silberstein SD, Schwedt TJ. The acute treatment of migraine in adults: the american headache society evidence assessment of migraine pharmacotherapies. Headache. 2015 Jan;55(1):3-20. doi: 10.1111/head.12499.
Results Reference
background
PubMed Identifier
16674762
Citation
Diener HC, Montagna P, Gacs G, Lyczak P, Schumann G, Zoller B, Mulder LJ, Siegel J, Edson K. Efficacy and tolerability of diclofenac potassium sachets in migraine: a randomized, double-blind, cross-over study in comparison with diclofenac potassium tablets and placebo. Cephalalgia. 2006 May;26(5):537-47. doi: 10.1111/j.1468-2982.2005.01064.x.
Results Reference
background
PubMed Identifier
31833000
Citation
Engel ER, Cheng J. IM ketorolac vs diclofenac potassium powder for oral solution for the acute treatment of severe migraine: a randomized controlled trial. Neurol Sci. 2020 Mar;41(3):537-542. doi: 10.1007/s10072-019-04157-y. Epub 2019 Dec 12.
Results Reference
derived

Learn more about this trial

IM Ketorolac vs Cambia for the Acute Treatment of Severe Migraine

We'll reach out to this number within 24 hrs