Abdominal Pain |
Pain, Abdominal |
Clinical Trial: Ziconotide Effectiveness and Safety Trial in Patients with Chronic Severe Pain
This study is currently recruiting patients.
|
Purpose
The purpose of this open-label study is to give chronic severe pain patients with existing intrathecal pump systems access to ziconotide.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Pain | Drug: Ziconotide | Phase III |
MedlinePlus related topics: Pain
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Expanded Access Assignment, Safety Study
Official Title: An Open-Label, Long-Term, Multi-Center, Intrathecal Ziconotide (PRIALT) Effectiveness and Safety Trial (ZEST) in Patients with Chronic Severe Pain
Expected Total Enrollment: 300
Study start: February 2004
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- Each patient must have chronic severe pain of malignant or nonmalignant etiology with inadequate pain relief from or intolerance to conventional therapy.
- Each patient must have a predicted life expectancy of greater than or equal to 6 weeks relative to baseline.
- Each patient must be able to respond to the Visual Analog Scale of Pain Intensity (VASPI).
- Each patient must have an implanted programmable SynchroMed infusion device or a CADD-Micro external programmable infusion device and spinal catheter (hereafter "IT pump and spinal catheter") prior to enrollment into this trial. (If a patient has an external pump, the Investigator must ensure that the patient is at a low risk for infection and that the patient is capable of maintaining good personal hygiene. The Investigator must have demonstrated the ability to successfully manage patients with external pumps prior to enrolling a patient in this trial.)
- Each patient must be at least 18 years of age.
- Each patient must be competent to give written informed consent and has given written informed consent prior to performance of any study-related procedures. Reasonable accomodation of visually impaired patients will be allowed.
- Each patient is willing and able to comply with the protocol requirements.
- Each female patient of childbearing potential must agree to use adequate contraceptive methods while on PRIALT as determine by the Investigator.
Exclusion Criteria:
- Presence of pregnancy or lactation.
- Participation in another investigational drug or device trial within the preceding 30 days.
- Presence of known hypersensitivity to PRIALT or any of its components.
- Presence of any contraindication to continued IT therapy (for example, infection at the pump or catheter externalization site, uncontrolled bleeding diathesis, spinal canal obstruction that impairs cerebrospinal fluid (CSF) circulation, or patient and caregiver inability to manage and protect the IT pump and spinal catheter system and return for clinic follow up visits).
- Presence of any condition (for example, psychosis, severe depression or suicidal ideation, homicidality, somatization disorder, active substance abuse, cognitive deficits, dementia or other serious medical or psychiatric condition) that in the Investigator's opinion precludes the patient's ability to participate in this study.
Location and Contact Information
Alabama
Alabama Pain Center, Huntsville, Alabama, 35801, United States; No longer recruiting
Center for Pain Management, Huntsville, Alabama, 35801, United States; No longer recruiting
Arizona
Outcomes Research International, Tucson, Arizona, 85712, United States; No longer recruiting
Otto Uhrik, MD, Sun City West, Arizona, 85373, United States; No longer recruiting
Arkansas
Innovative Spine Care, Little Rock, Arkansas, 72205, United States; No longer recruiting
The RC Goodman Pain Institute, Fort Smith, Arkansas, 72901, United States; No longer recruiting
California
Bay Area Pain Center, Los Gatos, California, 95032, United States; No longer recruiting
Galileo Surgery Center, San Luis Obispo, California, 93405, United States; No longer recruiting
Pacific Pain Treatment Centers, San Francisco, California, 94109, United States; No longer recruiting
Shreenath Clinical Services, Long Beach, California, 90807, United States; No longer recruiting
Shreenath Clinical Services, Lake Forest, California, 92630, United States; No longer recruiting
Shreenath Clinical Services, Beverly Hills, California, 90211, United States; No longer recruiting
Advanced Pain Institute, Duarte, California, 91010, United States; No longer recruiting
Pacific Pain Medicine Consultants, Oceanside, California, 92056, United States; No longer recruiting
Northridge Surgery & Pain Management Center, Northridge, California, 91324, United States; No longer recruiting
Colorado
Rocky Mountain Clinical Research, Golden, Colorado, 80401, United States; No longer recruiting
Pain Relief Center of Colorado, Arvada, Colorado, 80002, United States; No longer recruiting
Pain Care Specialists, Colorado Springs, Colorado, 80907, United States; No longer recruiting
Connecticut
Comprehensive Pain and Headache Treatment Centers, LLC, Derby, Connecticut, 06418, United States; No longer recruiting
Florida
Clinical Pharmacology Services, Tampa, Florida, 33617, United States; No longer recruiting
Sarasota Pain Associates, Sarasota, Florida, 34243, United States; No longer recruiting
Florida Institute of Medical Research, Jacksonville, Florida, 32207, United States; No longer recruiting
Space Coast Pain Institute, Merritt Island, Florida, 32953, United States; No longer recruiting
West Gables Rehabilitation Hospital, Miami, Florida, 33155, United States; No longer recruiting
Georgia
Shepherd Center, Inc., Atlanta, Georgia, 30309, United States; No longer recruiting
Comprehensive Pain Care, PC, Marietta, Georgia, 30060, United States; No longer recruiting
Illinois
The University of Chicago, Dept. of Surgery, Section of Neurosurgery, Chicago, Illinois, 60637, United States; No longer recruiting
Indiana
Indianapolis Neurosurgical Group, Indianapolis, Indiana, 46202, United States; No longer recruiting
Iowa
Des Moines Orthopedic Surgeons, West Des Moines, Iowa, 50266, United States; No longer recruiting
University of Iowa Health Care, Iowa City, Iowa, 52242, United States; No longer recruiting
Kentucky
Pain Control Network, PSC/PCN Surgical Suites, LLC, Louisville, Kentucky, 40205, United States; No longer recruiting
University of Kentucky, Lexington, Kentucky, 40536, United States; No longer recruiting
Michigan
Wayne State University - School of Medicine, Detroit, Michigan, 48201, United States; No longer recruiting
Minnesota
Medical Advanced Pain Specialists (MAPS), Minneapolis, Minnesota, 55433, United States; No longer recruiting
Mississippi
The Center for Pain Medicine, Hattiesburg, Mississippi, 39402, United States; No longer recruiting
Missouri
Pain Management Associates, Clinical Research, Independence, Missouri, 64055, United States; No longer recruiting
St. John's Regional Healthcare, Springfield, Missouri, 65804, United States; No longer recruiting
Nevada
Pain Management - Anesthesiology, Las Vegas, Nevada, 89117, United States; No longer recruiting
New Hampshire
Dr. O'Connell's Pain Care Centers, Inc., Somersworth, New Hampshire, 03878, United States; No longer recruiting
New York
All Island Pain Consultants, Bay Shore, New York, 11706, United States; No longer recruiting
Medical Pain Management of Central New York, Syracuse, New York, 13210, United States; No longer recruiting
Cohn Pain Management Center, Bethpage, New York, 11714, United States; No longer recruiting
Roswell Park Cancer Institute, Buffalo, New York, 14263, United States; No longer recruiting
New York Presbyterian Hospital/Cornell Medical Center, New York, New York, 10021, United States; No longer recruiting
NYU Pain Management Center, New York, New York, 10016, United States; No longer recruiting
North Carolina
Duke Medical Center Pain Clinic, Durham, North Carolina, 27705, United States; No longer recruiting
The Center for Clinical Research, Winston Salem, North Carolina, 27103, United States; No longer recruiting
Ohio
Cincinnati Centers for Pain Relief, Inc., Hamilton, Ohio, 45011, United States; No longer recruiting
Oklahoma
PETC Research Group, Inc., Tulsa, Oklahoma, 74137, United States; No longer recruiting
Oregon
Pain Management Consultants, PC, Portland, Oregon, 97225, United States; No longer recruiting
Pain Consultants of Oregon, Eugene, Oregon, 97401, United States; No longer recruiting
Pennsylvania
Lehigh Valley Hospital, Allentown, Pennsylvania, 18103, United States; No longer recruiting
Magee Rehabilitation, Philadelphia, Pennsylvania, 19102, United States; No longer recruiting
South Carolina
Carolinas Center for Advanced Management of Pain, Spartanburg, South Carolina, 29302, United States; No longer recruiting
South Dakota
Avera St. Luke's Hospital, Aberdeen, South Dakota, 57401, United States; No longer recruiting
Texas
Consultants In Pain Research, PA, San Antonio, Texas, 78217, United States; No longer recruiting
International Pain Institute, Lubbock, Texas, 79413, United States; No longer recruiting
The University of Texas Medical Branch, Galveston, Texas, 77555, United States; No longer recruiting
Dallas Spine Care P.A., Dallas, Texas, 75235, United States; No longer recruiting
Advanced Pain Medicine, Dallas, Texas, 75237, United States; No longer recruiting
American Pain & Wellness, PA, Plano, Texas, 75093, United States; No longer recruiting
Utah
Lifetree Clinical Research, Salt Lake City, Utah, 84106, United States; No longer recruiting
University of Utah Pain Management Center, Salt Lake City, Utah, 84108, United States; No longer recruiting
Virginia
Pain Management Center, University of Virginia, Charlottesville, Virginia, 22903, United States; No longer recruiting
West Virginia
The Center For Pain Relief, Charleston, West Virginia, 25301, United States; No longer recruiting
More Information
Record last reviewed: November 2004
Last Updated: December 9, 2004
Record first received: January 26, 2004
ClinicalTrials.gov Identifier: NCT00076544
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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