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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02993289
Other study ID # H-16029763
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 24, 2016
Est. completion date November 30, 2023

Study information

Verified date June 2020
Source Danish Headache Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Medication-overuse headache (MOH) is a disabling condition, yet treatable. According to European guidelines and based on evidence, multidisciplinary detoxification is the first choice of treatment for MOH. However, consensus about the details in such detoxification programs is lacking. Contrary, other headache specialists believe more in treating chronic headache with medication overuse with single-therapy of prophylaxis and no withdrawal of acute medication, based on randomized controlled double-blinded placebo trial with prophylaxes. Only a single RCT has compared single-therapy with prophylaxis to detoxification. However there was no significant difference.

AIM:

1. To compare three different treatment protocols in order to improve the therapy of MOH.

2. To test several baseline variables for being potential predictors for good treatment outcome.

3. To examine the role of epigenetics in MOH.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 115
Est. completion date November 30, 2023
Est. primary completion date July 2, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Patients with medication-overuse headache:

Inclusion Criteria:

- Confirmed MOH diagnosis according to the ICHD-III beta (1).

- Eligible for outpatient treatment based on type of medication overuse (without massive pure opioids and barbiturates overuse), and personal resources and motivation.

- Capable of completing headache diary/calendar.

- Age = 18 years old and capable of providing informed consent.

- Medication-overuse headache based on initial tension-type headache (TTH) or migraine.

- Signed informed consent.

Exclusion Criteria:

- Severe physical illness or psychiatric disorders.

- Addiction to alcohol or other drugs.

- Current treatment with headache prophylaxis. Patients can be included minimum 5 weeks after stop of prophylaxis.

- Pregnancy, breastfeeding or planned pregnancy within the next 12 months.

- Inability to provide reliable information about medical history.

Criteria for Control group 1 - Episodic migraineurs:

- Episodic migraine, with/without concomitant tension-type headache, according to the ICHD-III beta.

- Headache days / month = 6 at time of inclusion.

- Days with analgesics / month = 6 at time of inclusion.

- Prophylactics are allowed.

- Age = 18 years old.

- Ability to fill out headache calendar.

- No previous medication overuse.

- No significant co-morbid pain, physical or psychiatric disorders.

- No addiction to alcohol or drug-abuse.

- No pregnancy, breastfeeding or planned pregnancy within the next 12 months.

Criteria for Control group 2 - Healthy volunteers:

•= 2 days with headache in the past month at time of inclusion.

- Days with analgesics / month = 6 at time of inclusion.

- Age = 18 years old.

- No significant co-morbid pain, physical or psychiatric disorders.

- No addiction to alcohol or drug-abuse.

- No pregnancy, breastfeeding or planned pregnancy within the next 12 months.

Study Design


Intervention

Other:
Different well-known treatments


Locations

Country Name City State
Denmark Danish Headache Center Glostrup Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Danish Headache Center

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Difference in DNA-profile between patients with MOH and controlgroups. Baseline
Other Difference in methylation levels and RNA sequence analysis in patients with MOH undergoing treatment compared to controls. From baseline to 6 months follow-up
Other Analysis of association between methylation levels and treatment outcome defined as 1) reduction in headache days per month at 6 months and 12 months and 2) percent of cured vs. percent of relapsers after 12 months. At 6 and 12 months follow-up
Primary Reduction in headache days per month in group A and C compared to group B. Six months follow-up
Secondary Reduction in headache days per month Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Two and 12 months follow-up and 4 years
Secondary Reduction in days/month with use of analgesics and/or migraine medication. Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Two, 6 and 12 months follow-up and 4 years
Secondary Responders based on reduction in headache days / month (percentage with more than 30%, 50% and 75%). Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Two, 6 and 12 months follow-up and 4 years
Secondary Reduction in headache intensity. Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
This outcome will be presented as 1) Total headache intensity per month, and as 2) Visual Analogue Scale (VAS).
Two, 6 and 12 months follow-up and 4 years
Secondary Descriptive report of self-reported adverse effects of treatments. Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Two, 6 and 12 months follow-up
Secondary Changes in Headache Under-Response to Treatment (HURT)-score. Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Two, 6 and 12 months follow-up
Secondary Drop-out rate. One, 2, 4, 6, 9 and 12 months follow-up and 4 years
Secondary Changes in Hospital Anxiety and Depression Scale (HADS). Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Six and 12 months follow-up
Secondary Changes in Quality of Life (QoL) score. Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Six and 12 months follow-up
Secondary Changes in Severity of Dependence Score (SDS). Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Six and 12 months follow-up
Secondary Changes in Perceived Stress Score (PSS). Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Twelve months follow-up.
Secondary Patient's satisfaction questionnaire Group A and C versus group B.
Group A (detoxification with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Group B (single-therapy with prophylaxis) versus group C (detoxification with postponed prophylaxis).
Two, 6 and 12 months follow-up
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