Actively Recruiting
Pilot Study of the Osteo-Fluidic-Sensitive (OFS) in Tension-type Headache.
Led by Poitiers University Hospital · Updated on 2026-01-06
30
Participants Needed
1
Research Sites
195 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The hypothesis of the study is the Osteo-fluidic-Senstive is effective for lowering headache pains (Reduction of the number of days of headaches per month) for patients having frequent episodic tension-type headache. The OFS method will improve quality of life and will reduce the consumption of crisis treatments. Compare the efficacy of the Osteo-Fluidic-Sensitive method versus a placebo method on patients with tension type headache for the reduction of the number of days of headaches per month after 3 months of treatment at Centre Hospitalier Universitaire de Poitiers.
CONDITIONS
Official Title
Pilot Study of the Osteo-Fluidic-Sensitive (OFS) in Tension-type Headache.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 75 years
- Having frequent episodic tension-type headache (2 to 14 headache days per month) with or without migraine characteristics per International Classification of Headache Disorders 3rd edition
- Completed a headache diary the month before the study
- Understands and accepts the study effects
- Signed informed consent
- Has health insurance coverage
You will not qualify if you...
- Having other types of headaches such as chronic tension-type headache, migraines only, cluster headaches, or neuralgias
- Taking venlafaxine, gabapentin, duloxetine, clomipramine, or botulinum toxin treatments
- Participating in another clinical research study
- Pregnant or lactating women, or women of child-bearing age without effective contraception
- Individuals under reinforced protection (juvenile), deprived of liberty by justice or administrative decision, living in a sanitary or social establishment, adults under legal protection, or in critical medical conditions
AI-Screening
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Trial Site Locations
Total: 1 location
1
CHU Poitiers
Poitiers, France, 86000
Actively Recruiting
Research Team
H
Helene KERSUZAN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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