Trials / Withdrawn
WithdrawnNCT01325090
Early Administration of Botox® in Neuropathic Pain Due to Thoracoscopy or Thoracotomy
Early Administration of Botulinum Toxin Type A (Botox®) in Neuropathic Pain Due to Thoracoscopy or Thoracotomy: a Randomized, Double Blind, Placebo Controlled Study
- Status
- Withdrawn
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- University Hospital, Limoges · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Botulinum toxin type A has been reported to inhibit the release of various pain neurotransmitters (SP, CGRP, glutamate) responsible for neurogenic inflammation, a process that results from the sensitization of C-fiber nociceptors (peripheral sensitization). This action is probably responsible for the analgesic effect of botulinum toxin type A recently demonstrated in patients with neuropathic pain of peripheral origin.In those studies, patients had been suffering for years. The investigators can hypothesizes that earlier administration of Botox in the course of neuropathic pain might prevent central sensitization, that is secondary to peripheral sensitization. The investigators can hope to increase efficacy of Botulinum toxin type A injections and to prevent chronification of pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | BOTOX | A syringe of 1 ml contain 25 Allergan units. |
| OTHER | PLACEBO | The pharmacist will fill syringes in tuberculins of 1 ml with injectable solution of sodium chloride of 0,9 %. |
Timeline
- Start date
- 2011-05-01
- Primary completion
- 2013-11-01
- Completion
- 2014-11-01
- First posted
- 2011-03-29
- Last updated
- 2018-08-13
Source: ClinicalTrials.gov record NCT01325090. Inclusion in this directory is not an endorsement.