The purpose of this study is to determine if two sustained released formulations of carisoprodol are more effective than placebo.
Methodology: This will be a randomized, double-blind, double-dummy, placebo-controlled, parallel-group study in subjects 18-70 years of age with acute, painful, muscle spasm of the lower back. The study consists of a baseline screening (Study Day 1), during which subjects will be evaluated for inclusion/exclusion criteria, and a 7-day double-blind treatment period (Study Day 1 through Study Day 7). Subjects will be randomly assigned to be dosed twice daily with one of the following double-blind treatments: SR carisoprodol 500-mg tablets, SR carisoprodol 700-mg tablets, or placebo. Subjects will be evaluated in the clinic on Study Days 1, 3 and 7. Subjects who remain symptomatic on Study Day 7 will be allowed to continue in the study for a 7-day, double-blind extension period at the discretion of the Investigator. Subjects will be contacted by telephone for a safety follow-up 7 days after the last dose of study medication. A pharmacokinetic (PK) substudy will be conducted at selected sites. These sites will obtain blood samples for PK analysis at the end of the 7-day treatment period and the 14-day treatment period, if applicable.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
830
Subject Rated Change Relief From Starting Backache of Pain on a 100-point Visual Analog Scale
on a visual analog scale of 0 to 100 millimeters(mm) with 0 being no pain and 100 being maximum pain By measuring the amount of pain before and during treatment done at each visit and recording the difference in mm.During treatment scores were averaged and this average was compared to the baseline value.
Time frame: baseline to 14 days
Subject Functional Assessment Based on the Roland-Morris Disability Questionnaire (RMDQ)
Subject functional assessment based on the Roland-Morris Disability Questionnaire (RMDQ)at day 14.Subjects were asked to read a list of 24 sentences that people have used to describe themselves when they had back pain, and were asked to mark those statements that described their condition that day. The number of marked statements was added. A decrease in the number of marked statements from baseline represented improvement on the RMDQ.
Time frame: baseline and day +14
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Brookwood Internists, P.C.
Birmingham, Alabama, United States
Gulf Shores General Practice Center
Gulf Shores, Alabama, United States
Simon Williamson Clinic, PC
Hueytown, Alabama, United States
Vaugh H Mancha Jr., PC Family Practice
Montgomery, Alabama, United States
NextCare Institute for Clinical Research
Phoenix, Arizona, United States
HOPE Research Institute
Phoenix, Arizona, United States
Fiel Family and Sports Medicine
Tempe, Arizona, United States
Lynn Institute of the Ozarks
Little Rock, Arkansas, United States
Quality of life Medical, LLC
Anaheim, California, United States
ICT - Beverly Hills
Beverly Hills, California, United States
...and 63 more locations