Condition: Posttraumatic Headache · Sponsor: Danish Headache Center
The study is an investigator-initiated randomized, placebo-controlled, double-blind, parallelgroup trial. Eighty subjects with PTH will be included and randomized 1:1 for treatment with BTX-A or placebo (isotonic saline). The study comprises a 4-week baseline phase before injection of either active drug or placebo followed by a 12-week evaluation period. Treatment will be double-blind, and subjects will only receive one treatment cycle. Endpoints will be assessed in the evaluation period (weeks 5 to 8) compared to baseline (weeks -4 to -1).
This description comes directly from the study's public registry record.
Lucia Zavala, MD · 38632062 · lucia.jimena.zavala@regionh.dk
Henrik Schytz, MD · 38632062 · henrik.winther.schytz.01@regionh.dk
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| Danish Headache Center | Glostrup Municipality, Denmark | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06839118