Prospective Randomized Clinical Trial of Doxepin in Canine Laryngeal Paralysis: Dogs
The aim of this study is to evaluate client perception of quality of life improvement in Labrador Retrievers with laryngeal paralysis (LP) given doxepin for one month compared to dogs given placebo.
• Labrador Retrievers with clinical signs consistent with non-critical LP. To be evaluated for enrollment, dogs will have initial history and physical exam. If considered likely to have LP, dogs will have routine
hematologic, biochemical, and thyroid evaluation and then undergo an ultrasound of the larynx and laryngoscopy to confirm diagnosis.
• Unstable LP such that surgery is likely to be needed within the study period
• Serious co-morbidities that might affect laryngeal function or preclude completion of the study including untreated hypothyroidism, neoplasia, severe heart disease, severe renal or liver disease.
• History of urine retention, glaucoma or severe cardiac disease
• Administration of drugs known to potentiate serotonin syndrome
Reduced initial exam charge. No charge for blood work, echolaryngography, and study medication for enrolled dogs. The client is responsible for all other charges. A $100 account credit will be given at completion of study.
Jill Sammarco, BVSc, MRCVS, DACVS
RBVH Surgery Department (Tinton Falls)
Eric N. Glass, MS, DVM, DACVIM (Neurology)
RBVH Neurology & Neurosurgery Department