Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04140734
Other study ID # 2019-10410
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2021
Est. completion date July 2027

Study information

Verified date January 2024
Source Montefiore Medical Center
Contact Anne Barmettler, MD
Phone (978) 886-7122
Email abarmett@montefiore.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine which of three types of spacer grafts (hard palate vs autologous ear cartilage vs Enduragen) are the most effective in lower eyelid retraction repair outcomes as measured by MRD2 (margin to reflex distance 2)


Description:

Lower eyelid retraction is a common eyelid malposition, typically caused by thyroid eye disease, excessive resection of skin in a cosmetic lower eyelid blepharoplasty, vertical rectus muscle recession, facial nerve paralysis, or a normal anatomical variant.[1] When the lower eyelid is displaced inferiorly, exposing sclera between the limbus and the eyelid margin, symptoms can vary from ocular irritation and discomfort to vision threatening corneal decompensation. If medical management does not suffice, surgery is indicated. Although lower eyelid retractor lysis alone has been described, supporting material (spacer graft) placed to augment the posterior lamella is generally required for more effective elevation of the eyelid.[2] Various materials have been utilized, including autologous auricular cartilage, bovine acellular dermal matrix, porcine acellular dermal matrix, hard palate mucosa, dermis and dermis fat grafts. Previous studies on acellular dermal matrix use in lower eyelid retraction repair consist of retrospective efficacy studies with only 2 comparative studies. However, conflicting results raised doubt as to which material was superior. In addition, a prospective, randomized comparative study of spacer grafts used for lower eyelid retraction repair was done comparing autologous auricular cartilage, porcine acellular dermal matrix, and bovine acellular dermal matrix. The results yielded no statistically significant difference in surgical outcomes and complications.[3]. As of now, surgery with any of the spacer grafts, including autologous hard palate, is accepted as standard of care. [4] This study is designed to determine whether using hard palate as a spacer graft will have statistically significant different surgical outcomes and complications as compared to autologous ear cartilage and porcine acellular dermal matrix spacer grafts. Although studied separately, this has not been studied before in a prospective randomized manner and may prove to demonstrate improved surgical results and decreased complications. This can guide future choice of spacer graft used in lower eyelid retraction repair surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date July 2027
Est. primary completion date July 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients will be included if they undergo lower eyelid retraction repair requiring a spacer graft between July 1, 2019 and July 1, 2022 . Exclusion Criteria: - Patients will be excluded if they are younger than 18 years old, required concurrent surgeries (e.g., midface lift or full thickness skin graft) or required further surgeries on the operated eyelid within the 6 months postoperatively. In addition, patients with less than 1-month follow up will be excluded from all outcome analysis and those without postoperative 6-month data will be excluded from the postoperative month 6 MRD2 calculation.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Spacer Graft
In this prospective, randomized clinical trial, patients who will already be undergoing lower eyelid retraction repair with a spacer graft will randomly be assigned via a randomization web-site to receive 1 of 3 spacer grafts: hard palate, autologous auricular cartilage, and porcine acellular dermal matrix (Enduragen). Both the patient and the surgeon will know which of the three possible grafts are being used.

Locations

Country Name City State
United States Montefiore Medical Center Bronx New York

Sponsors (1)

Lead Sponsor Collaborator
Montefiore Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary MRD2 (margin to reflex distance 2) Analyzing the effectiveness of the spacer grafts with respect to lower eyelid retraction repair. MRD2 is the distance in millimeters between the pupillary light reflex and the lower eyelid margin with the patient looking at a light reflex in primary gaze. 6 months post-op
Secondary Post-Surgical Complications Conjunctival injection and eyelid swelling will be graded by the examiner on a scale of 0 to 10. Tearing, itching, discomfort will be graded by the patient on a scale of 0 to 10 both pre-operatively and post-operatively. 6 months post-op
See also
  Status Clinical Trial Phase
Completed NCT01190397 - Warming Efficiency of Warm Compresses Versus BLEPHASTEAM® in Eyelid Therapy Phase 1
Withdrawn NCT05672407 - The Role of Local Tranexamic Acid on Periorbital Oculoplastic Surgery Phase 4
Completed NCT03199911 - Topical Antibiotic Prophylaxis for Eyelids Phase 4
Recruiting NCT04689230 - Small Incision Technique Versus Upper Blepharoplasty in Upper Eyelid Medial Pad Fat Removal N/A
Completed NCT01091311 - Evaluation of Satisfaction Regarding Patient's Management of Ocular Surface Diseases Phase 4
Recruiting NCT04359979 - Tamsulosin for Thyroid Lid Retraction N/A
Recruiting NCT04102878 - Transconjunctival vs Transcutaneous Anaesthesia in Oculoplastics N/A
Completed NCT01189474 - Evaluation of Satisfaction Regarding Patient's Management of Ocular Surface Diseases Phase 4
Active, not recruiting NCT04149210 - FLuorometholone as Adjunctive MEdical Therapy for TT Surgery (FLAME) Trial Phase 3
Not yet recruiting NCT04235803 - Telemedicine Follow-up for Routine, Low-Risk Oculoplastic Surgery N/A
Completed NCT04554329 - Bandage Contact Lenses Versus Eye Patching of Müller's Muscle-conjunctival Resection N/A
Recruiting NCT04898933 - Patient Satisfaction After Eyelid Lesion Excision
Recruiting NCT04861454 - Brassiere Brow Suture and Internal Browpexy
Recruiting NCT04255667 - Eyelid Crush for Marginal Eyelid Surgery
Recruiting NCT04201925 - Functional Changes After Upper Blepharoplasty
Recruiting NCT05750251 - Effect of Upper Eyelid Surgeries on Corneal Characteristics
Recruiting NCT05016362 - Medial Fat Pad Preservation in Upper Eyelid Blepharoplasty
Recruiting NCT05945069 - Feasibility of Dynamic Muscle Stimulation + Radiofrequency for Improving Blink Quality in Subjects With Dry Eye Disease N/A
Recruiting NCT04720586 - Surgical Treatment of Lower Eyelid Involutional Entropion and Dermatochalasis N/A
Recruiting NCT04921020 - Assessment of Eyelid Topology and Kinetics Based on Deep Learning Method