Silver Nitrate Application and Topical Corticosteroids for Hypergranulation Tissue

Last updated: May 28, 2015
Sponsor: Akron Children's Hospital
Overall Status: Trial Status Unknown

Phase

4

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT02398539
150110
  • Ages < 18
  • All Genders

Study Summary

This protocol describes a randomized, two arm clinical trial comparing two topical treatments in patients with hypergranulation tissue at gastrostomy tube sites. The subjects are randomized to either group 1or group 2 treatments:

Maximum duration of therapy is 4 weeks. However, the therapy may be discontinued anytime at the discretion of the investigator or if there is resolution of the of the hypergranulation tissue.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Pediatric patients <18

  2. Evaluated for hypergranulation at the G-tube site

  3. Inpatient and out-patient

Exclusion

Exclusion Criteria: Children not meeting the above criteia

Study Design

Total Participants: 50
Study Start date:
April 01, 2015
Estimated Completion Date:
April 30, 2016

Connect with a study center

  • Akron Children's Hospital

    Akron, Ohio 44308
    United States

    Active - Recruiting

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