Prosthetic Motility and Complications in Pegged Versus Unpegged Hydroxyapatite Orbital Implants

Anophthalmos Clinical Trial

Status Active, not recruiting

Clinical Trial Summary

Pegging the hydroxyapatite for increasing prosthetic motility sometimes leads to some complications for the patient. These complications ranging from discharge, granuloma formation, exposure, implant infection to socket discomfort and etc. We are going to compare prosthetic motility, objectively and subjectively (patients satisfaction) before and after pegging the hydroxy- apatite, and evaluate the complications after pegging.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Anophthalmos
• Orbital Implants

• NCT number: NCT00371280
• Study type: Interventional
• Source: hahid Beheshti University of Medical Sciences
• Status: Active, not recruiting
• Phase: Phase 2/Phase 3
• Start date: November 2005
• Completion date: November 2006