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Zinc as an Adjunctive Therapy for Cervical Dystonia
Evaluation of Supplemental Zinc as an Adjunct to Prolong the Duration of Benefit After Botulinum Toxin Injections in Subjects With Cervical Dystonia
Who can join
Ages 18 to 89 · All sexes
Full eligibility criteria
Inclusion Criteria: * Adults aged 18-89 years. * Diagnosed with cervical dystonia. * Receiving regular BoNT type A (Botox) injections for at least six months. Exclusion Criteria: * Known allergy or intolerance to zinc. * Significant comorbidities or concurrent medications that could interfere with study outcomes. * Pregnant or breastfeeding women. * Already taking a zinc supplement which would exceed tolerable upper intake level in adults (40 mg elemental zinc per day) with addition of zinc study supplement.
About the study
The goal of this clinical trial is to evaluate if supplemental zinc can prolong the duration of benefit of botulinum toxin injections in cervical dystonia patients receiving care at the University of Florida.
The main aims are:
1. To evaluate the efficacy of zinc citrate supplementation in prolonging the duration of symptom relief provided by botulinum toxin type A (Botox) injections in cervical dystonia patients. 2. To assess the safety and tolerability of zinc supplementation in this patient population. 3. To analyze the potential influence of zinc supplementation on the quality of life and functional outcomes in cervical dystonia patients receiving Botox.
Researchers will compare zinc citrate to a placebo (a look-alike substance that contains no active drug) to see if zinc works to extend the effects of Botox.
Participants will:
Take zinc citrate or a placebo every day for 3 months, then cross over to the alternative treatment for another 3 months.
Visit the clinic every 3 months for Botox injections, check ups and surveys.
What is being tested
- Zinc citrate (drug)
- Placebo (drug)
Sponsor: University of Florida · Participants: 25 · Started: Jun 1, 2026
Contact the study team
- Julie Segura, BA · Phone: 352-733-2412
Official record on ClinicalTrials.gov — NCT07140874
Locations in the U.S.
| Florida | Norman Fixel Institute for Neurological Diseases, Gainesville |
Conditions
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.