search
Back to results

Comparison of Two Detoxification Protocols for Treatment of Medication-overuse Headache (MUM)

Primary Purpose

Medication-overuse Headache

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Detoxification
Sponsored by
Danish Headache Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Medication-overuse Headache

Eligibility Criteria

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

Inclusion Criteria:

  • MOH-diagnosis according to ICHD-3beta
  • Eligible for out-patient care
  • Previously diagnosed with primary headache forms.

Exclusion Criteria:

  • Previously diagnosed with secondary headache forms
  • Significant physical or psychiatric illness
  • Pregnancy or breastfeeding
  • Inadequate language skills to follow the patient education and filling out questionnaires.

Sites / Locations

  • Danish Headache Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Protocol A

Protocol B

Arm Description

In program A, patients underwent detoxification without any acute medication during a two months period (complete stop of acute medication intake).

In program B, patients were allowed to take up to 2 days a week with analgesics or migraine medication during the two months detoxification period (restricted acute medication intake).

Outcomes

Primary Outcome Measures

Headache frequency

Secondary Outcome Measures

Days with acute medication/ month
Headache frequency
Headache intensity (Total intensity per month meassured by headache calendars).
Patients daily register headache intensity by 0,1, 2 or 3 corresponding to the intensity. The headache intensity is summed up for 30 days.
Scores from questionnaires Headache Under-Response to Treatment (HURT)
Scores from questionnaires Hospital Anxiety and Depression Score (HADS)
Scores from questionnaires World Health Organization Quality of Life score
Scores from questionnaires Severity of Dependence Score (SDS)
Scores from questionnaires Dolo-score

Full Information

First Posted
September 1, 2016
Last Updated
July 20, 2018
Sponsor
Danish Headache Center
search

1. Study Identification

Unique Protocol Identification Number
NCT02903329
Brief Title
Comparison of Two Detoxification Protocols for Treatment of Medication-overuse Headache
Acronym
MUM
Official Title
Efficacy of Restricted Acute Medication Intake Compared to no Acute Medication Intake During a Two Months Detoxification Period in Medication-overuse Headache
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
June 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Danish Headache Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Medication-overuse headache (MOH) is a common, costly and disabling disorder affecting approximately 63 million people worldwide. MOH is a potentially treatable condition, and there are different opinions among headache specialists concerning the correct treatment strategy. The study is a prospective longitudinal open-label randomized controlled study comparing two detoxification programs conducted in a tertiary headache care center. Patients with MOH are either randomized to treatment in program A or program B. In program A, patients undergo detoxification without any acute medication during a two months period (complete stop of acute medication intake). In program B, patients was allowed to take up to 2 days a week with analgesics or migraine medication during the two months detoxification period (restricted acute medication intake). Both A and B are out-patient programs, and patients in both groups receive patient education, consisting of six lessons, managed by specialized headache nurses in collaboration with specialized psychologists and physiotherapists (Figure 1). All patients are also offered rescue medication (levomepromazine or promethazine) and antiemetics, if necessary. The need for prophylactic treatment is evaluated individually after 2-month detoxification. Patients are followed-up at 2, 6 and 12 months after detoxification. All patients are asked to continuously register headache calendar and to fulfill questionnaires at all the follow-up visits. In addition they are asked to fill out questionnaires (Headache Under-Response to Treatment (HURT), Hospital Anxiety and Depression Score (HADS), Severity of Dependence Score (SDS), World Health Organization Quality of Life Score(WHO QoL) and Dolo-score) at baseline, 2, 6 and 12 months
Detailed Description
Patients with contact to Danish headache center are recruited consecutively. The MOH-diagnosis is based on least 3 months previous detailed history and at least 1 month fulfilled headache diary or headache calendar prior to the visit. Patients were allocated to either program A or B by a concealed randomization process. The patients were randomized in blocks of 10 by use of opaque, sealed envelopes. Statistics Statistical Package for Social Sciences (SPSS) version 22 is used for statistical calculations. Continuous variables are presented as mean (SD) and median (25-75 percentiles). For normal distributed continuous variables the investigators use paired and unpaired student's T-test, while for skewed distribution the investigators used Mann-Whitney test. Categorical variables is presented as percentage (N), and analyzed by chi-square test. All results are shown as intention-to-treat (ITT). The p-value is two-sided and p ≤ 0.05 is considered as significant. The primary outcome is reduction in headache days per month. Clinical relevant difference is estimated to 20% between the two groups. The standard deviation based on previous published literature was estimated to 35%. Accepting an alfa-error on 5% and 80% power, 80 patients are needed. Based on previous studies, it is assumed that the drop-out rate will be approximately 15-20%. Therefore the investigators aim to include 100 patients corresponding to 50 in each group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Medication-overuse Headache

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Protocol A
Arm Type
Active Comparator
Arm Description
In program A, patients underwent detoxification without any acute medication during a two months period (complete stop of acute medication intake).
Arm Title
Protocol B
Arm Type
Active Comparator
Arm Description
In program B, patients were allowed to take up to 2 days a week with analgesics or migraine medication during the two months detoxification period (restricted acute medication intake).
Intervention Type
Other
Intervention Name(s)
Detoxification
Other Intervention Name(s)
Treatment for MOH
Intervention Description
Two ways of composing the detoxification protocol
Primary Outcome Measure Information:
Title
Headache frequency
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Days with acute medication/ month
Time Frame
6 and 12 month
Title
Headache frequency
Time Frame
12 months
Title
Headache intensity (Total intensity per month meassured by headache calendars).
Description
Patients daily register headache intensity by 0,1, 2 or 3 corresponding to the intensity. The headache intensity is summed up for 30 days.
Time Frame
6 and 12 months
Title
Scores from questionnaires Headache Under-Response to Treatment (HURT)
Time Frame
6 and 12 months
Title
Scores from questionnaires Hospital Anxiety and Depression Score (HADS)
Time Frame
6 and 12 months
Title
Scores from questionnaires World Health Organization Quality of Life score
Time Frame
6 and 12 months
Title
Scores from questionnaires Severity of Dependence Score (SDS)
Time Frame
6 and 12 months
Title
Scores from questionnaires Dolo-score
Time Frame
6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: MOH-diagnosis according to ICHD-3beta Eligible for out-patient care Previously diagnosed with primary headache forms. Exclusion Criteria: Previously diagnosed with secondary headache forms Significant physical or psychiatric illness Pregnancy or breastfeeding Inadequate language skills to follow the patient education and filling out questionnaires.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louise Ninett Carlsen, MD
Organizational Affiliation
Danich Headache Center, Neurological department, Rigshospitalet-Glostrup
Official's Role
Study Chair
Facility Information:
Facility Name
Danish Headache Center
City
Glostrup
State/Province
Copenhagen
ZIP/Postal Code
2600
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30732459
Citation
Nielsen M, Carlsen LN, Munksgaard SB, Engelstoft IMS, Jensen RH, Bendtsen L. Complete withdrawal is the most effective approach to reduce disability in patients with medication-overuse headache: A randomized controlled open-label trial. Cephalalgia. 2019 Jun;39(7):863-872. doi: 10.1177/0333102419828994. Epub 2019 Feb 7.
Results Reference
derived
PubMed Identifier
29050498
Citation
Carlsen LN, Munksgaard SB, Jensen RH, Bendtsen L. Complete detoxification is the most effective treatment of medication-overuse headache: A randomized controlled open-label trial. Cephalalgia. 2018 Feb;38(2):225-236. doi: 10.1177/0333102417737779. Epub 2017 Oct 19.
Results Reference
derived

Learn more about this trial

Comparison of Two Detoxification Protocols for Treatment of Medication-overuse Headache

We'll reach out to this number within 24 hrs