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Clinical Trial Summary

The goal of this randomized controlled study in Thailand. is to find if there is a role of local anesthetic greater occipital nerve block at Cervical spine level 2 under ultrasound guide in prophylaxis of episodic migraine and chronic migraine in patients with failed oral prophylaxis medication. According to guidelines of the International Headache Society for controlled trials of preventive treatment of migraine attacks in episodic and chronic migraine,the primary and secondary outcome were monitoring followed by these research guideline After informed consent, volunteer will be stratified random into 2 groups of injection agent at unilateral greater occipital nerve block on headache site under US guide by pain physician - Normal saline - 0.5% bupivacaine the injection was done 2 times between Week 0 and week 4 as to wean off placebo effect the volunteer will be monitor by pain diary at 1 month before intervention at week 0,4,8,12 and follow up at week 24 for Migraine Disability Assessment Test (MIDAS) ,Thai Hospital-Anxiety-depression index(Thai-HADS)


Clinical Trial Description

- Neurologist screening candidate volunteers for this study, following the inclusion and exclusion criteria - Candidate volunteers attended pain clinic for he protocol detail about this research and informed consent - After signing consent, Volunteers would be stratified randomization into 2 groups between Normal saline and bupivacaine - Volunteers would be done base line headache diary for 1 month before performing the procedure (Week -4 to week0) - At Week 0, Volunteers would be applied local anesthetic cream at skin injection site before done the procedure - According to stratified randomization, Pain interventionist and also volunteers would be blinded to the group - First Unilateral greater occipital nerve block at Cervical spine level 2 (C2) was done under ultrasound guide (Week0) - Telemedicine Follow up at week 2 - Second Unilateral greater occipital nerve block at C2 level was done under ultrasound guide (Week4) - Volunteers would be follow up via telemedicine and done headache diary until 3 months after 1st injection - Volunteers would be follow up according to outcome monitoring protocol in Week 0,4,8,12,24 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06432127
Study type Interventional
Source Mahidol University
Contact RAVIWON ATISOOK, M.D.
Phone +66819140784
Email raviwon.ati@gmail.com
Status Not yet recruiting
Phase Phase 4
Start date May 30, 2024
Completion date January 2027

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