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A Study To Evaluate Methods To Evaluate Back Pain

NCT01045993 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2013-04-01

Study results available
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Summary

The study is designed to assess methods used in clinical research.

Conditions

Interventions

DEVICE

Heat Device

8-Hour Heatwrap

DEVICE

Sham Device

Inactive wrap worn for 8 hours

DRUG

marketed analgesic

2 x 200 mg ibuprofen tablets

DRUG

Placebo

2 x placebo tablets

Sponsors & Collaborators

  • Wyeth is now a wholly owned subsidiary of Pfizer

    lead INDUSTRY

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2010-07-31
Completion
2010-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01045993 on ClinicalTrials.gov