Overview

The Use of Botox in Advanced Parkinson's Patients Experiencing Pain

Status:
Unknown status
Trial end date:
2015-09-01
Target enrollment:
0
Participant gender:
All
Summary
Most Parkinsonism related pain can be assigned to one or more of five categories: musculoskeletal pain, neuritic or radicular pain, dystonia associated pain, primary or central pain, and akathitic discomfort. In PD pain tends to affect the side of the body that was initially, or more severe affected by the motor symptoms. Botulinum toxins are an effective treatment modality for a growing number of neurological conditions. They have been studied for a variety of conditions associated with PD including dystonia, jaw tremor, apraxia of eyelid opening, camptocormia, dyskinesias, freezing of gait, sialhorrea, overactive bladder and constipation. There are no studies for the use of Botulinum Toxin for pain in PD. The investigators will perform a double-blind, randomized cross-over study evaluating the efficacy and safety of an individual pattern of BTXA injections targeted at painful muscles vs. placebo injection.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Health Network, Toronto
Treatments:
Botulinum Toxins
Criteria
Inclusion Criteria:

- Subjects with advanced PD (Hoehn and Yahr 3-5) and painful limbs not responding to
antiparkinsonian agents sufficiently.

- BTXA treatment naÃ-ve patients or not received any within last 12 months (including
other indications).

- Stable PD and pain medications for at least 30 days

- Competence to self-report pain severity in a Visual Analogue Scale (VAS)

Exclusion Criteria:

- Subjects with a primary cause of pain unrelated with PD and associated with another
medical condition e.g. severe arthritis

- Subjects that because of the severity or refractory pain are under an unfixed
analgesic schedule

- Subjects unable to self- report pain severity in a VAS

- Subjects undergoing acute infections or other acute intercurrences.

- Any contraindication to receiving BTXA injections:

1. Subjects who are hypersensitive to any BTXA or to any ingredient in the
formulation or component of the container (Clostridium Botulinum toxin type A
neurotoxin complex 900 kD, Human Serum Albumin and Sodium Chloride).

2. The presence of infection at the proposed injection site(s).