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Study on the Safety and Efficacy of Nitric Oxide Gel in Subjects With Pressure Sore

NCT01351493 · Status: UNKNOWN · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2012-07-11

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy of nitric oxide gel for pressure sore recovery.

Conditions

  • Pressure Ulcer

Interventions

DRUG

Nitric Oxide

Nitric Oxide Gel, once or twice per day, 12weeks

DRUG

placebo

placebo Gel, once or twice per day, 12weeks

Sponsors & Collaborators

  • China Medical University Hospital

    lead OTHER

Principal Investigators

  • Chiu-Shong Liu, M.D. · China Medical University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2013-07-31
Completion
2013-07-31

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Drugs

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 NCT01351493 on ClinicalTrials.gov