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To Evaluate the Therapeutic Efficacy of Hydrated Amniotic Membrane in Promoting Closure of Refractory Macular Holes.

Primary Purpose

Macular Holes

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Hydrated Amniotic Membrane Plug
ILM filling
Conventional ILM peeling
Sponsored by
Oriental Neurosurgery Evidence-Based-Study Team
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Macular Holes

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. idiopathic macular hole was defined as macular hole diameter (with no history of secondary macular hole) larger than 800μm in minimum linear diameter ;
  2. Patients with an idiopathic macular hole submitted to pars plana vitrectomy with internal limiting membrane peeling treatment without closing it and macular hole diameter larger than 200μm.

Patients who meet any of 1/2 and signed informed consent can be included. Note: if both eyes of the subject meet the inclusion criteria, the investigator decides which eye should be included.

Exclusion Criteria:

  1. idiopathic macular hole diameter less than 800μm in minimum linear diameter;
  2. Macular hole caused by trauma and laser;
  3. Macular holes secondary to another vitreoretinal diseases;
  4. Macular hole of pathological myopia (axial length ≥26.0mm and diopter ≥6.00D,posterior scleral staphyloma,the atrophic choroid and retina with scleral exposure);
  5. Known to be allergic to amniotic membrane.

    Patients with any of the following eye diseases:

  6. Patients with other ocular disease (diabetic retinopathy, glaucoma, uveitis, ocular tumors, etc);
  7. Macular hole of other causes (secondary);
  8. History of vitreoretinal surgery for a condition other than the idiopathic macular hole (retinal detachment, vitreous hemorrhage);

    Patients with any of the following eye conditions:

  9. Using systemic drugs that are toxic for the optic nerve or retina (chloroquine, hydroxychloroquine, tamoxifen, ethambutol, etc);
  10. Patients with ocular surgery.

Sites / Locations

  • Tianjin Medical University General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Hydrated Amniotic Membrane Plug

ILM filling

Conventional ILM peeling

Arm Description

Patients suffering from refractory macular holes as documented by spectral-domain OCT will undergo pars plan vitrectomy with Hydrated Amniotic Membrane insertion into the macular hole.

The ILM filling technique, in which free ILM is plug into the macular hole area

Peeling with complete removal of the internal limiting membrane within the vascular arch

Outcomes

Primary Outcome Measures

Rate of Anatomic closure
Rate of anatomic macular hole closure in the OCT at month 6
Reconstruction of the foveal layered retinal structure change
Change in the reconstruction of the foveal layered retinal structure by OCT at 1, 3, and 6 months

Secondary Outcome Measures

amniotic membrane dislocation
conform amniotic membrane dislocation in the OCT and/or binocular indirect ophthalmoscope at day 1 and 7
BCVA change
change in the BCVA at Preoperative,1, 3, and 6 months
Retinal capillary plexus density change
change in the retinal capillary plexus density with OCT-A at Preoperative,1, 3, and 6 months

Full Information

First Posted
May 24, 2022
Last Updated
May 27, 2022
Sponsor
Oriental Neurosurgery Evidence-Based-Study Team
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1. Study Identification

Unique Protocol Identification Number
NCT05396209
Brief Title
To Evaluate the Therapeutic Efficacy of Hydrated Amniotic Membrane in Promoting Closure of Refractory Macular Holes.
Official Title
Multicenter Case Control Clinical Trials to Compare the Healing Process of Refractory Macular Hole With Different Surgical Techniques
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2022 (Anticipated)
Primary Completion Date
May 15, 2024 (Anticipated)
Study Completion Date
June 15, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oriental Neurosurgery Evidence-Based-Study Team

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To compare anatomic and functional results, and to evaluate postoperatively the healing process in 3 different techniques for the closure of the refractory macular holes (MH).
Detailed Description
The aim of the study is to evaluate the therapeutic efficacy of Hydrated Amniotic Membrane in promoting closure of refractory macular holes. The Hydrated Amniotic Membrane has been used in some cases as an adjunct in the macular holes closure and as a substrate for cell growth and improvement of visual acuity. Hydrated Amniotic Membrane is supposed to promote epithelialization and have anti-fibrotic, anti-inflammatory properties. In the present study, the patients who meet the inclusion criteria will be randomized and undergo pars plana vitrectomy surgery with peeling of the ILM and a fragment of the ILM itself or an amniotic membrane plug will be put in place. The patients included in the study will undergo a complete eye examination, including corrected Visual Acuity measurement (BCVA), performing the Optical Coherence Tomography (OCT) and/or microperimetry, multifocal electroretinogram (mfERG) in the pre-operative. Patients will undergo surgery after complementary exams and adequate pre-anesthetic evaluation. Patients will be evaluated on the 1st and 7th postoperative days and at 1, 3, and 6 months after surgery. The patient will undergo a complete eye examination and postoperative follow-up as described above, and during visits on the 1st and 7th day, and in the 1st, 3th and 6th month of the postoperative period, BCVA and OCT will be performed and/or the microperimetry, multifocal electroretinogram (mfERG) will be performed in the 1st, 3th and 6th postoperative month for evaluation and monitoring of anatomical and functional responses, respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Macular Holes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hydrated Amniotic Membrane Plug
Arm Type
Active Comparator
Arm Description
Patients suffering from refractory macular holes as documented by spectral-domain OCT will undergo pars plan vitrectomy with Hydrated Amniotic Membrane insertion into the macular hole.
Arm Title
ILM filling
Arm Type
Active Comparator
Arm Description
The ILM filling technique, in which free ILM is plug into the macular hole area
Arm Title
Conventional ILM peeling
Arm Type
Active Comparator
Arm Description
Peeling with complete removal of the internal limiting membrane within the vascular arch
Intervention Type
Procedure
Intervention Name(s)
Hydrated Amniotic Membrane Plug
Intervention Description
Using Hydrated Amniotic Membrane plug with vitrectomy to try to close refractory macular hole
Intervention Type
Procedure
Intervention Name(s)
ILM filling
Intervention Description
The ILM filling technique - Rossi et al show that ILM filling technique was more efficacious in closing full-thickness macular holes larger than 630μm, in which the free ILM after peeling is plug into the area of the macular hole
Intervention Type
Procedure
Intervention Name(s)
Conventional ILM peeling
Intervention Description
Peeling with complete removal of the internal limiting membrane within the vascular arch
Primary Outcome Measure Information:
Title
Rate of Anatomic closure
Description
Rate of anatomic macular hole closure in the OCT at month 6
Time Frame
Month 6 post operative
Title
Reconstruction of the foveal layered retinal structure change
Description
Change in the reconstruction of the foveal layered retinal structure by OCT at 1, 3, and 6 months
Time Frame
Month 1, 3, 6 post-operative
Secondary Outcome Measure Information:
Title
amniotic membrane dislocation
Description
conform amniotic membrane dislocation in the OCT and/or binocular indirect ophthalmoscope at day 1 and 7
Time Frame
DAY 1,7 post operative
Title
BCVA change
Description
change in the BCVA at Preoperative,1, 3, and 6 months
Time Frame
Time Frame: Preoperative,Month 1, 3, 6 post operative
Title
Retinal capillary plexus density change
Description
change in the retinal capillary plexus density with OCT-A at Preoperative,1, 3, and 6 months
Time Frame
Preoperative,Month 1, 3, 6 post operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: idiopathic macular hole was defined as macular hole diameter (with no history of secondary macular hole) larger than 800μm in minimum linear diameter ; Patients with an idiopathic macular hole submitted to pars plana vitrectomy with internal limiting membrane peeling treatment without closing it and macular hole diameter larger than 200μm. Patients who meet any of 1/2 and signed informed consent can be included. Note: if both eyes of the subject meet the inclusion criteria, the investigator decides which eye should be included. Exclusion Criteria: idiopathic macular hole diameter less than 800μm in minimum linear diameter; Macular hole caused by trauma and laser; Macular holes secondary to another vitreoretinal diseases; Macular hole of pathological myopia (axial length ≥26.0mm and diopter ≥6.00D,posterior scleral staphyloma,the atrophic choroid and retina with scleral exposure); Known to be allergic to amniotic membrane. Patients with any of the following eye diseases: Patients with other ocular disease (diabetic retinopathy, glaucoma, uveitis, ocular tumors, etc); Macular hole of other causes (secondary); History of vitreoretinal surgery for a condition other than the idiopathic macular hole (retinal detachment, vitreous hemorrhage); Patients with any of the following eye conditions: Using systemic drugs that are toxic for the optic nerve or retina (chloroquine, hydroxychloroquine, tamoxifen, ethambutol, etc); Patients with ocular surgery.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Qihua Wang, MD
Phone
86-10-18601180961
Email
wqha01696@btch.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hua Yan, MD,PhD
Organizational Affiliation
Ophthalmology of Tianjin Medical University General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tianjin Medical University General Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300052
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Qihua Wang, MD
Phone
86-10-18601180961
Email
wqha01696@btch.edu.cn
First Name & Middle Initial & Last Name & Degree
Hua Yan, MD, PhD
Phone
86-22-60817010
Email
zyyyanhua@tmu.edu.cn

12. IPD Sharing Statement

Learn more about this trial

To Evaluate the Therapeutic Efficacy of Hydrated Amniotic Membrane in Promoting Closure of Refractory Macular Holes.

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