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RECRUITING
NCT07140874
PHASE2

Zinc as an Adjunctive Therapy for Cervical Dystonia

Sponsor: University of Florida

View on ClinicalTrials.gov

Summary

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.

Official title: Evaluation of Supplemental Zinc as an Adjunct to Prolong the Duration of Benefit After Botulinum Toxin Injections in Subjects With Cervical Dystonia

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2026-02-20

Completion Date

2026-12-31

Last Updated

2026-03-09

Healthy Volunteers

No

Interventions

DRUG

Zinc citrate

Oral zinc citrate 30 mg daily

DRUG

Placebo

Placebo

Locations (1)

Norman Fixel Institute for Neurological Diseases

Gainesville, Florida, United States