Silver Nitrate Application and Topical Corticosteroids for Hypergranulation Tissue

Overview

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.

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Central Contacts