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Verapamil vs. Sertraline for Vestibular Migraine & Chronic Subjective Dizziness

Primary Purpose

Vestibular Migraine, Chronic Subjective Dizziness

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Verapamil
Sertraline
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Vestibular Migraine focused on measuring migraine variant, chronic dizziness, pharmacologic dissection

Eligibility Criteria

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

Inclusion criteria:

  1. Neurotologic diagnoses of both vestibular migraine and chronic subjective dizziness
  2. All other co-existing medical or psychiatric conditions are stable, and no greater than moderate severity
  3. Able to complete study assessments in person and by phone
  4. Able to travel to Mayo Clinic, Rochester, Minnesota for first and last study visits
  5. Willing to avoid pregnancy during study (abstinence or acceptable birth control)

Exclusion criteria:

  1. Presence of any other active neurotologic diagnoses
  2. Medical or psychiatric conditions that would preclude or confound study drugs
  3. Use of medications or supplements that would preclude or confound study drugs
  4. Past treatment of headache or dizziness with a full trial of a calcium channel blocker or selective serotonin reuptake inhibitor
  5. Allergy to verapamil or sertraline

Sites / Locations

  • Mayo Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Verapamil

Sertraline

Arm Description

Verapamil extended release oral tablets administered in a flexible dose format ranging from 120 mg to 360 mg daily, as determined by severity of headache and dizziness.

Sertraline oral tablets administered in a flexible dose format ranging from 25 mg to 150 mg daily depending on severity of headache and dizziness.

Outcomes

Primary Outcome Measures

2-week Average Rating of Severity of Headache from the Daily Symptom Diaries
Daily ratings of headache will be evaluated at 2 week intervals for 12 weeks.
2-week Average Rating of Severity of Dizziness/Unsteadiness from the Daily Symptom Diaries
Daily ratings of dizziness/unsteadiness will be evaluated at 2 week intervals for 12 weeks.
2-week Average Rating of Sensitivity to Motion of Self from the Daily Symptom Diaries
Daily ratings of sensitivity to motion of self will be evaluated at 2 week intervals for 12 weeks.
2-week Average Rating of Sensitivity to Motion in the Environment from the Daily Symptom Diaries
Daily ratings of sensitivity to motion in the environment will be evaluated at 2 week intervals for 12 weeks.
2-week Average Rating of Difficulty of Performing Precision Visual Tasks from the Daily Symptom Diaries
Daily ratings of difficulty of performing precision visual tasks will be evaluated at 2 week intervals for 12 weeks.

Secondary Outcome Measures

Mean Number of Acute Attacks Per Two Week Period
Acute attacks will be assessed every 2 weeks for 12 weeks.
Mean Score of Dizziness Handicap Inventory (DHI)
Dizziness related handicap will be assessed every 4 weeks for 12 weeks. The Dizziness Handicap Inventory (DHI) consists of 25 questions, with a total possible score ranging from 0 (no dizziness) to 50 (severe dizziness).
Mean Score of Migraine-Specific Quality of Life (MSQ)
Quality of life related to headache will be assessed at 4 week intervals for 12 weeks. The Migraine-Specific Quality of Life 2.1 (MSQ) consists of 14 items, with a total possible score ranging from 14 (affected none of the time) to 84 (affected all of the time).

Full Information

First Posted
August 14, 2012
Last Updated
August 20, 2015
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT01669304
Brief Title
Verapamil vs. Sertraline for Vestibular Migraine & Chronic Subjective Dizziness
Official Title
Pharmacologic Dissection of Vestibular Migraine and Chronic Subjective Dizziness: A Double-Blind Parallel Group Trial Comparing Response to Verapamil Versus Sertraline
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
August 2012 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Vestibular migraine (VM) and chronic subjective dizziness (CSD) commonly cause vertigo, unsteadiness and dizziness. Clinical investigators are studying these illnesses to understand them better. VM and CSD occur together in about 1/3 of patients. That makes it hard to diagnose them accurately and decide what treatments to use. As a result, doctors and patients may be confused about these diagnoses. The goal of this study was use two different medications to tease apart the symptoms of VM and CSD. Patients who have VM and CSD together were given either verapamil or sertraline for 12 weeks. These medications are used to treat VM and CSD, though they are not approved for this purpose. Verapamil is believed to have stronger effects on symptoms of VM. Sertraline is believed to have stronger effects on symptoms of CSD. By comparing the responses of patients to these two medications, the researchers hoped to learn more about the key features of VM and CSD.
Detailed Description
Chronic dizziness and recurrent vertigo are frequent complaints in primary and specialty medical care settings. Two common causes of these symptoms are vestibular migraine (VM) and chronic subjective dizziness (CSD), which may be seen in up to 25% of patients examined in tertiary neurotology centers. However, VM and CSD are relatively new diagnoses that have not yet been validated. Furthermore, recent research found that they co-exist 30% of the time with overlap in several features. From a clinical standpoint, this makes it difficult to diagnose and treat them well. From a research standpoint, it confounds subject selection for mechanistic investigations. The primary goal of this study was to dissect VM and CSD in order to identify the key features and clarify the diagnostic criteria of each condition. Subjects diagnosed with coexisting VM-CSD were treated with either verapamil or sertraline. It was hypothesized that a differential treatment response to these two pharmacologic probes would help to tease apart the unique clinical features of VM and CSD and identify risk factors that are shared or separate between the two conditions. It was hoped that the different mechanisms of action of the two study medications might also shed light on the physiologic underpinnings of VM and CSD. This project was a 14-week, prospective, randomized, double-blind, parallel group, pharmacologic dissection (PD) trial. A 12-week treatment period followed 2 weeks of baseline observation. Patients charted daily headache and vestibular symptoms. VM and CSD symptoms and potential confounds such as anxiety and depression were measured at two week intervals. Data were analyzed for differential and shared treatment effects that align with or oppose current concepts of VM and CSD. A PD trial uses response to one or more pharmaceutical probes (drugs) to study physiologic mechanisms of illness. A PD trial may provide data to separate overlapping manifestations of comorbid illnesses. This is useful for conditions that lack biomarkers. It also may provide data to identify characteristics of illnesses (symptoms, signs, cellular processes) that are associated with specific pharmacologic mechanisms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Migraine, Chronic Subjective Dizziness
Keywords
migraine variant, chronic dizziness, pharmacologic dissection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Verapamil
Arm Type
Experimental
Arm Description
Verapamil extended release oral tablets administered in a flexible dose format ranging from 120 mg to 360 mg daily, as determined by severity of headache and dizziness.
Arm Title
Sertraline
Arm Type
Experimental
Arm Description
Sertraline oral tablets administered in a flexible dose format ranging from 25 mg to 150 mg daily depending on severity of headache and dizziness.
Intervention Type
Drug
Intervention Name(s)
Verapamil
Other Intervention Name(s)
Calan SR, Covera-HS, Isoptin SR, Verelan PM
Intervention Type
Drug
Intervention Name(s)
Sertraline
Other Intervention Name(s)
Zoloft
Primary Outcome Measure Information:
Title
2-week Average Rating of Severity of Headache from the Daily Symptom Diaries
Description
Daily ratings of headache will be evaluated at 2 week intervals for 12 weeks.
Time Frame
Week 0 to Week 12
Title
2-week Average Rating of Severity of Dizziness/Unsteadiness from the Daily Symptom Diaries
Description
Daily ratings of dizziness/unsteadiness will be evaluated at 2 week intervals for 12 weeks.
Time Frame
Week 0 to Week 12
Title
2-week Average Rating of Sensitivity to Motion of Self from the Daily Symptom Diaries
Description
Daily ratings of sensitivity to motion of self will be evaluated at 2 week intervals for 12 weeks.
Time Frame
Week 0 to Week 12
Title
2-week Average Rating of Sensitivity to Motion in the Environment from the Daily Symptom Diaries
Description
Daily ratings of sensitivity to motion in the environment will be evaluated at 2 week intervals for 12 weeks.
Time Frame
Week 0 to Week 12
Title
2-week Average Rating of Difficulty of Performing Precision Visual Tasks from the Daily Symptom Diaries
Description
Daily ratings of difficulty of performing precision visual tasks will be evaluated at 2 week intervals for 12 weeks.
Time Frame
Week 0 to Week 12
Secondary Outcome Measure Information:
Title
Mean Number of Acute Attacks Per Two Week Period
Description
Acute attacks will be assessed every 2 weeks for 12 weeks.
Time Frame
Week 0 to Week 12
Title
Mean Score of Dizziness Handicap Inventory (DHI)
Description
Dizziness related handicap will be assessed every 4 weeks for 12 weeks. The Dizziness Handicap Inventory (DHI) consists of 25 questions, with a total possible score ranging from 0 (no dizziness) to 50 (severe dizziness).
Time Frame
Week 0 to Week 12
Title
Mean Score of Migraine-Specific Quality of Life (MSQ)
Description
Quality of life related to headache will be assessed at 4 week intervals for 12 weeks. The Migraine-Specific Quality of Life 2.1 (MSQ) consists of 14 items, with a total possible score ranging from 14 (affected none of the time) to 84 (affected all of the time).
Time Frame
Week 0 to Week 12
Other Pre-specified Outcome Measures:
Title
Mean score for Dizziness on the Sheehan Disability Scale/Migraine Disability Assessment Scale (SDS-MIDAS)
Description
Dizziness symptoms will be assessed at 2 week intervals for 12 weeks. The Sheehan Disability Scale/Migraine Disability Assessment Scale (SDS-MIDAS) consists of 5 questions, with a total possible score ranging from 0 (no disability) to 72 (extremely disruptive).
Time Frame
Week 0 to Week 12
Title
Mean score for Headache on the Sheehan Disability Scale/Migraine Disability Assessment Scale (SDS-MIDAS)
Description
Headache symptoms will be assessed at 2 week intervals for 12 weeks. The Sheehan Disability Scale/Migraine Disability Assessment Scale (SDS-MIDAS) consists of 5 questions, with a total possible score ranging from 0 (no disability) to 72 (extremely disruptive).
Time Frame
Week 0 to Week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Neurotologic diagnoses of both vestibular migraine and chronic subjective dizziness All other co-existing medical or psychiatric conditions are stable, and no greater than moderate severity Able to complete study assessments in person and by phone Able to travel to Mayo Clinic, Rochester, Minnesota for first and last study visits Willing to avoid pregnancy during study (abstinence or acceptable birth control) Exclusion criteria: Presence of any other active neurotologic diagnoses Medical or psychiatric conditions that would preclude or confound study drugs Use of medications or supplements that would preclude or confound study drugs Past treatment of headache or dizziness with a full trial of a calcium channel blocker or selective serotonin reuptake inhibitor Allergy to verapamil or sertraline
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey Staab, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17309987
Citation
Staab JP, Ruckenstein MJ. Expanding the differential diagnosis of chronic dizziness. Arch Otolaryngol Head Neck Surg. 2007 Feb;133(2):170-6. doi: 10.1001/archotol.133.2.170.
Results Reference
background
PubMed Identifier
19134491
Citation
Ruckenstein MJ, Staab JP. Chronic subjective dizziness. Otolaryngol Clin North Am. 2009 Feb;42(1):71-7, ix. doi: 10.1016/j.otc.2008.09.011.
Results Reference
background
PubMed Identifier
21799457
Citation
Eggers SD, Staab JP, Neff BA, Goulson AM, Carlson ML, Shepard NT. Investigation of the coherence of definite and probable vestibular migraine as distinct clinical entities. Otol Neurotol. 2011 Sep;32(7):1144-51. doi: 10.1097/MAO.0b013e31822a1c67.
Results Reference
background
Links:
URL
http://clinicaltrials.mayo.edu/clinicaltrialdetails.cfm?trial_id=101873
Description
additional research information from Mayo Clinic

Learn more about this trial

Verapamil vs. Sertraline for Vestibular Migraine & Chronic Subjective Dizziness

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