HOME  | CONTACT  | PATIENT LOGIN  | CLINIC LOGIN  | FAQ
  • PATIENTS &
    HEALTHY VOLUNTEERS
  • INVESTIGATORS
  • CROS / SPONSORS
  • CAREERS
  • TRIAL ALERTS

TRIALS SEARCH
      
  • HEALTH NEWS

  • RSS FEEDS

  • ABOUT TRIALS

  • LINK TO US


View Clinical Trial (Medical Research Study)


A Randomized, Double-Blind, Placebo-Controlled Study Of A Fixed Dose Of Subcutaneous Methylnaltrexone In Adults With Advanced Illness And Opioid-Induced Constipation: Efficacy, Safety, And Additional Health Outcomes

Signup
Browse Studies

City:   Mobile
State:   Alabama
Zip Code:   36604
Conditions:   Opioid-Induced Constipation
Purpose:   This study will evaluate the safety and efficacy of methylnaltrexone administered as subcutaneous injections in subjects who have opioid-induced constipation and an advanced illness. The hypothesis is that methylnaltrexone will be safe and effective in relieving opioid-induced constipation in these subjects.
Study Summary:  
Criteria:   Inclusion Criteria: - Is an adult 18 years of age or older - Has a diagnosis of advanced illness (ie, a terminal illness such as incurable cancer or other end-stage disease) - Has a life expectancy of at least 1 month. - Is receiving opioids on a regular schedule (not just as-needed or rescue doses) for the control of pain or discomfort for at least 2 weeks before the first dose of study drug. - Has constipation that is caused by opioid medications. Exclusion Criteria: - Has a known or suspected allergy to methylnaltrexone or other similar compounds (e.g. naltrexone or naloxone). - Has a known or suspected mechanical gastrointestinal obstruction. - Has any potential nonopioid cause of bowel dysfunction that might be a major contributor to the constipation. - Has any other clinically important abnormalities as determined by the investigator that may interfere with his or her participation in or compliance with the study. - Receiving opioid antagonist or partial antagonist products.
NCT ID:   NCT00672477
Primary Contact:   Study Director
Bob Rolleri
Salix Pharmaceuticals

Dave Mathews
Phone: 919-862-1000
Email: dave.mathews@salix.com
Backup Contact:   N/A
Location Contact:   Mobile, Alabama 36604
United States



There is no listed contact information for this specific location.

Site Status: Completed

Data Source:   ClinicalTrials.gov
Date Processed:   June 18, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
Click to view Full Listing


If you would like to be contacted by the clinical trial representative please enter your contact information, then click "I Am Interested In This Study"
First Name:  
Last Name:  
Email Address:  
Confirm Email:    
Daytime Phone (eg. 555-555-5555):  
City:  
State:
Zip Code:    
Best Time to Call:  
Questions/Comments:  
  • NEARBY STUDIES

Within 25 Miles

Chronic Low Back Pain - Mobile AL

Low Back Pain and Constipation - Mobile AL

Within 50 Miles

Postherpetic Neuralgia (Post-shingles pain) - Ocean Springs MS

Low Back Pain and Constipation - Foley AL

Low Back Pain and Constipation - Gulf Shores AL

Pediatric Migraines (Ages 12-17) - Ocean Springs MS

Within 100 Miles

Chronic Low Back Pain - Biloxi MS

COPD (Emphysema and Chronic Bronchitis) - Pensacola FL

COPD (Emphysema and Chronic Bronchitis) - Pensacola FL

COPD (Emphysema and Chronic Bronchitis) - Biloxi MS

 
Clinical Connections Home | Investigators | CROs / Sponsors | Clinical Trials Notification | Search Clinical Trials | About Clinical Trials | Links | Terms And Conditions | Sitemap | Suggestions / Feedback
© 1998-2013 | All trademarks are property of their legal owners. | All Rights Reserved

ClinicalConnection.com is a resource that provides individuals with information regarding clinical trials that are being conducted worldwide.

ClinicalConnection.com does not conduct these clinical trials nor endorse them. Please consult your doctor or physician before participating.