Evaluation of the Efficacy of the Osteo-Fluidic-sensitive (OFS) Versus Placebo Method in the Management of Frequent Episodic Tension-type Headache. Pilot Study.

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: t
View:

• 18 and 75 years' old

• Person having highly frequent episodic tension type headache (between 2 and 14 days of headaches per month) associated or not to headache with characteristic of a migraine per International Classification of Headache Disorders 3rd edition criteria

• Person who completed his headache agenda the month before the study.

• Patient who understands and accepts the effects of the study

• Signed consent

• Person with health insurance coverage

Locations
Other Locations
France
CHU Poitiers
RECRUITING
Poitiers
Contact Information
Primary
Helene KERSUZAN
helene.kersuzan@chu-poitiers.fr
+33549443961
Time Frame
Start Date: 2022-11-29
Estimated Completion Date: 2026-08-29
Participants
Target number of participants: 30
Treatments
Experimental: Osteo-Fluidic-Sensitive method
Placebo_comparator: Placebo method
Related Therapeutic Areas
Sponsors
Leads: Poitiers University Hospital

This content was sourced from clinicaltrials.gov