An Open-Label Extension Study of NGX-4010 for the Treatment of Neuropathic Pain
This study has been terminated.
Sponsor:
NeurogesX
Information provided by:
NeurogesX
ClinicalTrials.gov Identifier:
NCT00089557
First received: August 6, 2004
Last updated: June 23, 2005
Last verified: September 2004
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
This study is an open-label, multicenter, extension study for subjects who completed NeurogesX Study C111 and received treatment with NGX-4010 (Capsaicin Patch) within 12 weeks (up to +7days) before entry into Study C114
| Condition | Intervention | Phase |
|---|---|---|
|
Herpes Zoster Neuralgia Pain HIV Infections Peripheral Nervous System Diseases Diabetic Neuropathies Diabetes Mellitus Polyneuropathies |
Drug: Capsaicin Dermal Patch |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Masking: Open Label Primary Purpose: Treatment |
| Official Title: | An Open-Label Extension Study of NGX-4010 for the Treatment of Neuropathic Pain |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
Diabetes
Diabetic Nerve Problems
HIV/AIDS
Neurologic Diseases
Peripheral Nerve Disorders
Shingles
Drug Information available for:
Capsaicin
U.S. FDA Resources
Further study details as provided by NeurogesX:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Key Eligibility Criteria:
- Must have completed NeurogesX Study C111 and received treatment with NGX-4010 (Capsaicin Patch) within 12 weeks (up to +7 days) before entry into Study C114.
- Demonstrated adherence to protocol requirements during Study C111, and willing and able to comply with protocol requirements for the duration of the study participation.
- Must not have had any serious adverse experience since enrollment in Study C111, whether or not considered to be study drug-related.
- Must have intact skin at the treatment area.
- Must be prepared to remain on the same pain medications at the same doses as before the study for the entire duration of the study (36 weeks).
- Must not use topical pain medications on painful areas.
- Must be at least 18 years old, not pregnant, and able to take care of self independently, with only occasional assistance if needed.
- No history or current problem with substance abuse.
Contacts and Locations
No Contacts or Locations Provided
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00089557 History of Changes |
| Other Study ID Numbers: | C114 |
| Study First Received: | August 6, 2004 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by NeurogesX:
|
Dermal assessment Pain assessment Diary Analgesics Capsaicin Herpes zoster Neuralgia |
Pain HIV Infections Peripheral Nervous System Diseases Diabetic Neuropathies Diabetes Mellitus Polyneuropathies Complementary Therapies |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Diabetes Mellitus Diabetic Neuropathies Herpes Zoster Nervous System Diseases Neuralgia Peripheral Nervous System Diseases Polyneuropathies Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases |
Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Neuromuscular Diseases Diabetes Complications Herpesviridae Infections DNA Virus Infections Pain Neurologic Manifestations Signs and Symptoms Capsaicin Sensory System Agents |
ClinicalTrials.gov processed this record on June 18, 2013