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To study the success rate of evisceration with Hydroxyapatite orbital implant compared with Polymethylmethacrylate orbital implant

To study the success rate of evisceration with Hydroxyapatite orbital implant compared with Polymethylmethacrylate orbital implant

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20181127003
Enrollment
40
Registered
2018-11-27
Start date
2018-12-18
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients who has to undergo evisceration in conditions of endophthalmitis&#44

Interventions

A group of 20 patients undergo evisceration with hydroxyapatite orbital implant,A group of 20 patients undergo evisceration with PMMA orbital implant
Experimental Device,Experimental Device
evisceration with hydroxyapatite orbital implant,evisceration with polymethylmethacrylate

Sponsors

Faculty of medicine, Chulalongkorn university
Lead Sponsor
None, None
Collaborator

Eligibility

Sex/Gender
All
Age
15 Years to 90 Years

Inclusion criteria

Inclusion criteria: -A patient attendind Chulalongkorn hospital who has to undergo evisceration with inclusion criteria of severe corne ulcer, panophthalmitis , endophthalmitis, painful blind eye, phthisis bulbi. -A patient with more than 15 years of age

Exclusion criteria

Exclusion criteria: -A patient suspected of orbital mass or carcinoma. -A patients with severe disfigured orbital bone -A patient who underwent eyelid surgery or orbital surgery -A patient with medical conditions that is unable to perform surgery under general anesthesia. -A patient who undergoes evisceration without orbital implantation

Design outcomes

Primary

MeasureTime frame
Success rate 2 month Able to put on a prosthesis ,Success rate 2 month Able to put on a prosthesis

Secondary

MeasureTime frame
Complication rate 2 month To measure extrusion, exposure rate , Infection rate,Volume, motiity 2 month With hertel exophthalmometry, orbital and prosthesis motility from primary position

Contacts

Public ContactSuppapong Tirakunwichcha

Faculty of medicine, Chulalongkorn university

suppapong@gmail.com0840259111

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026