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Search / Trial NCT01251211

Botulinum Toxin in Peripheral Neuropathic Pain

Launched by HOSPITAL AMBROISE PARÉ PARIS · Nov 30, 2010

Trial Information

Current as of May 06, 2025

Completed

Keywords

Botulinum Toxin Neuropathic Pain Randomized Controlled Trial

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Men or women aged 18 to 85 years Spontaneous pain with a minimal intensity of 4/10 on numerical scle Pain present for at least 6 months Pain related to painful mononeuropathy or sensory polyneuropathy Able to understand the protocol and comply to the requirements of the study Written informed consent Painful area limited to a maximum of 240 cm2
  • Exclusion Criteria:
  • Facial pain Litigation (pending) Unstable condition responsible for neuropathic pain (ie, unstable immunological disease...) HIV or chemotherapy induced neuropathy Contraindications to BTX-A (neuromuscular disease, hypersensitivity, infection, coagulation disorder, pregnancy) Other pain more severe than neuropathic pain No compliance with the self diary Drug abuse or alcoholism Severe major depression Cognitive impairment Other research protocol within the last 30 days

About Hospital Ambroise Paré Paris

Hospital Ambroise Paré in Paris is a leading healthcare institution dedicated to advancing medical research and patient care. As a clinical trial sponsor, it focuses on innovative therapeutic approaches and cutting-edge treatments across various medical fields. The hospital is committed to fostering collaboration among multidisciplinary teams of healthcare professionals, researchers, and clinical experts to enhance the quality of clinical trials. With a strong emphasis on patient safety and ethical standards, Hospital Ambroise Paré aims to contribute significantly to the development of new medical therapies that improve patient outcomes and advance the field of medicine.

Locations

Limoges, , France

Sao Paulo, , Brazil

Boulogne Billancourt, , France

Patients applied

0 patients applied

Trial Officials

Nadine ATTAL, MD PhD

Study Director

APHP and INSERM

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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