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Long-term outcome of a newly designed supratarsal platinum weight for the correction of paralytic lagophthalmos

Long-term outcome of a newly designed supratarsal platinum weight for the correction of paralytic lagophthalmos: a prospective cohort study

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220802007
Enrollment
18
Registered
2022-08-02
Start date
2022-09-01
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

Paralytic lagophthalmos Peripheral facial nerve palsy Platinum weight, gold weight, lid loading, lagophthalmos, facial nerve palsy

Interventions

The new model platinum weight is in semi-elliptical shape. It consists of 2 holes on the inferior side for suturing to the tarsal plate. The length and height vary with the mass of the weight. For exa
Experimental Device
New design platinum weight

Sponsors

Office of Research Affairs, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male or female adults aged over 18 years old with diagnosis of paralytic lagophthalmos 2. Has an indication to perform lid loading, including but not limited significant lagophthalmos on gentle closure, etiology of facial paralysis that permanently precludes recovery of nerve function, exposure keratitis, significant ocular surface symptom due to lagophthalmos, and epiphora due to failed pumping mechanism in incomplete blinking.

Exclusion criteria

Exclusion criteria: None Patients that are lost to follow-up will be treated as censors and not excluded.

Design outcomes

Primary

MeasureTime frame
Long-term complication 2 years Incidence rate

Secondary

MeasureTime frame
Blink, gentle, forced lagophthalmos pre-operative, 1 month, 6 months mm,Time of delayed eyelid closure pre-operative, 1 month, 6 months seconds,upper eyelid contour and weight prominence pre-operative, 1 month, 6 months quality grading by two blinded assessors,Best corrected visual acuity pre-operative, 1 month, 6 months LogMAR,Tear break-up time pre-operative, 1 month, 6 months seconds,Corneal staining pre-operative, 1 month, 6 months fluoresceine staining,Visual function-related quality of life pre-operative, 6 months NEI-VFQ25 questionnaire

Countries

Thailand

Contacts

Public ContactPreamjit Saonanon

Faculty of Medicine, Chulalongkorn University

drpreamjit@gmail.com022564000

Outcome results

None listed

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