Efficacy of Aurosling in Frontalis Sling Suspension Surgery

NCT00753831 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2012-07-12

No results posted yet for this study

Summary

To Study the Efficacy of Aurosling as a suspension material in Frontalis suspension surgery in ptosis

Conditions

  • Ptosis, Eyelid

Interventions

PROCEDURE

Aurosling

Silicon rod to be used in frontalis suspension surgery

Sponsors & Collaborators

  • Aurolab

    lead OTHER

Principal Investigators

  • Usha Kim, DO, Dip NB · Aravind Eye Hospital, Madurai

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2009-07-31
Completion
2009-08-31

Countries

  • India

Study Locations

More Related Trials

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 NCT00753831 on ClinicalTrials.gov