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Clinical Trials/NCT06118190
NCT06118190CompletedNot Applicable

The Effectiveness of Mesotherapy (Lidocaine and Proxicam) in the Treatment of Chronic Migraine

Kanuni Sultan Suleyman Training and Research Hospital1 site in 1 country27 target enrollmentStarted: January 1, 2019Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
27
Locations
1
Primary Endpoint
Visual Analog Scale (VAS)

Study Overview

Brief Summary

Mesotherapy is a type of injection frequently used in clinics. It is a treatment procedure that involves the injection of some drugs under the skin or into the skin. Mesotherapy is used in musculoskeletal system diseases, but it is reported that the effects of its use in migraine are uncertain.

Detailed Description

Migraine is one of the types of headaches. For the diagnosis of chronic migraine, the headache must last more than 15 days. Nerve blocks, oral medication and neuromodulation are recommended for migraine treatment.Mesotherapy is a type of injection frequently used in clinics. It is a treatment procedure that involves the injection of some drugs under the skin or into the skin. Mesotherapy is used in musculoskeletal system diseases, but it is reported that the effects of its use in migraine are uncertain. This study was planned to show the effectiveness of mesotherapy in patients with migraine.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Masking Description

open label

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Clinical diagnosis of chronic migraine disease

Exclusion Criteria

  • Infection disease
  • Thyroid disease
  • Anemia disease
  • Systemic disease

Arms & Interventions

mesotherapy

Experimental

All participants who received mesotherapy were monitored regularly for the following three months to assess their prognosis and ensure patient adherence to treatment.

Intervention: Lidocain (Drug)

Outcomes

Primary Outcomes

Visual Analog Scale (VAS)

Time Frame: 12 th week

VAS rates pain on a scale of zero to 10. It is explained to the participant that 10 points means unbearable pain, zero points means no pain, and the patient is asked to rate his pain between zero and ten. Higher scores indicate increased pain severity

The frequency of painful days per month

Time Frame: 12th week

The participant is asked how many days she/he feels pain in a month.Higher numbers indicate increased frequency of painful days

Secondary Outcomes

  • Duration of attack per month(12th week)
  • the number of analgesic per month(12th week)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Elif Ozyigit

Principal Investigator

Kanuni Sultan Suleyman Training and Research Hospital

Study Sites (1)

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