Reconstruction of Upper Eyelid With a Newly Modified Cutler-Beard Technique With Tarsoconjunctival Graf

Reconstructive Surgical Procedure Clinical Trial

Official title:

Reconstruction of Upper Eyelid Defects Secondary to Malignant Tumors With a Newly Modified Cutler-Beard Technique With Tarsoconjunctival Graft

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03712995
• Other study ID #: RUE-2018
• Status: Completed
• Phase: N/A
• Start date: January 1, 2011
• Est. completion date: December 31, 2016

Study information

• Verified date: October 2018
• Source: Hospital Universitario 12 de Octubre
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To study the results of a modified Cutler-Beard technique , using a contralateral tarsoconjunctival graft, in patients who underwent excision of large malignant tumors of the upper eyelid

Description:

A tarsoconjunctival graft was harvested from the contralateral upper eyelid, with an extra 3 mm of conjunctiva from the superior edge of tarsus and was attached to the upper eyelid defect, differently than previously described.

Functional, cosmetic outcomes and postoperative complications were evaluated.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: December 31, 2016
• Est. primary completion date: December 31, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Upper eyelid defect after tumor resection

Exclusion Criteria:

• previous surgery

Related Conditions & MeSH terms

• Reconstructive Surgical Procedure

Intervention

Procedure:
• 'Cutler-Beard modified with graft'
A tarsoconjunctival graft was harvested from the contralateral upper eyelid, with an extra 3 mm of conjunctiva from the superior edge of tarsus and was attached to the upper eyelid defect, differently than previously described.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Hospital Universitario 12 de Octubre

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Symptoms of the patients	Number of symptoms referred by the patient, being 0 the best result	42 months
Primary	Eyelid retraction	Upper eyelid retraction in mm	42 months
Secondary	Retraction of the donor lower eyelid	Lower eyelid retraction in mm	42 months
Secondary	Lagophthalmos	Excessive aperture of the eyelids, in mm	42 months
Secondary	Lid margin stability	in mm	42 months
Secondary	Eyelid status	Number of complications, being 0 the best result	42 months