NCT06200727

Brief Summary

The goal of this clinical trial is to observe the role of PRF in treating ophthalmic diseases.The efficacy and safety of PRF were validated for four ophthalmic conditions: macular hole, pterygium, corneal ulcer, and patients undergoing trabeculectomy for glaucoma. The main question aims to answer is PRF's effectiveness in ocular surface and fundus diseases. Participants will be divided into 2 groups, the experimental group will be treated with PRF and the control group will be treated with conventional surgery, with a 12-month postoperative follow-up to determine the role of PRF on wound healing in ophthalmic diseases.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
170

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2023

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

December 11, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 11, 2024

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

January 12, 2024

Status Verified

January 1, 2024

Enrollment Period

2.5 years

First QC Date

December 11, 2023

Last Update Submit

January 11, 2024

Conditions

Keywords

PRF; pterygium; macular hole; corneal ulcer

Outcome Measures

Primary Outcomes (4)

  • Whether the macular hole is closed in participants with macular hole(Unit: yes/no)

    Using optical coherence tomography(OCT )to see if the macular hole is healing to compare the healing rate between the PRF membrane filling group and the ILM peeling group.

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

  • Whether the wound heals completely after pterygium excision in participants with pterygium(Unit: yes/no)

    Observation of the anterior segment of the eye using a slit lamp to determine whether the wound is healed after pterygium excision and to compare the healing rate between the PRF membrane-covered group and the autologous conjunctival-covered group.

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

  • IOP in participants undergoing trabeculectomy for glaucoma(Unit: mmHg)

    Measurement of IOP using an IOP meter to compare the effect of IOP reduction in glaucoma treatment in the PRF membrane group and the amniotic membrane group.

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

  • Whether the corneal ulcer is healing in participants with corneal ulcer(Unit: yes/no)

    The investigators use a slit lamp to examine the anterior segment of the eye to assess the corneal wound healing rate. The PRF membrane-covered group is compared to the control group.

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

Secondary Outcomes (4)

  • Best-corrected visual acuity (BCVA) in participants with macular hole(Unit: logMAR)

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

  • Occurrence of complications in participants with pterygium(Unit: rate)

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

  • Degree of tissue scarification in participants undergoing trabeculectomy for glaucoma(Unit: mild, moderate, severe)

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

  • Occurrence of complications in participants with corneal ulcer(Unit: rate)

    Pre-operation, and at 1 week, 1 month, 3 months, and 6 months post-operation.

Study Arms (8)

PRF membrane in macular hole

EXPERIMENTAL

To observe the healing and visual recovery of a macular hole, the macular hole was filled with a PRF membrane. Before the participant went into the operating theatre, a blood sample was taken from the anterior elbow vein using a 5 ml tube without anticoagulants. The middle layer of blood after centrifugation was PRF. After retrobulbar anesthesia and removal of the posterior vitreous cortex. In the PRF group, PRF membrane was utilized to fill the macular hole after the ILM was peeled. Then the eyeball was filled with sterile air after adequate air-liquid exchange. At the end of the operation, tobramycin dexamethasone ophthalmic ointment was applied to the operated eye with pressure, and the participant was instructed to maintain a prone position for 7 days after the operation.

Procedure: PRF membrane tamponade surgery in macular hole

Internal limmiting membrane(ILM) peeling in macular hole

ACTIVE COMPARATOR

After retrobulbar anesthesia and removal of the posterior vitreous cortex, the control group underwent the procedure of peeling the ILM. The ILM was completely removed from the retina. Then the eyeballs were filled with sterile air after adequate air-liquid exchange. At the end of the operation, tobramycin dexamethasone ophthalmic ointment was applied to the operated eye with pressure, and the participant was instructed to maintain a prone position for 7 days after the operation.

Procedure: ILM peeling in macular hole

PRF membrane transplantation in pterygium

EXPERIMENTAL

Following the removal of the pterygium, the prepared PRF was cut to match the size of the exposed scleral surface. It was then placed on the sclera and secured to the surrounding conjunctiva using 3-7 interrupted sutures of 10-0 nylon thread. This was done to ensure that the PRF implant was perfectly aligned with the conjunctiva.

Procedure: PRF membrane grafting in pterygium

Autologous conjunctival transplantation in pterygium

ACTIVE COMPARATOR

After the pterygium removal surgery, to restore the eye, participants need to undergo a corneal limbal stem cell transplant. The transplanted stem cells should be the same size as the exposed scleral surface above the temporal part of the eye. When transferring the transplant, ensured that the corneal edge of the grafted conjunctival flap was positioned opposite to the cornea. Closed the flap to the peripheral conjunctiva with 3-7 interrupted sutures using 10-0 nylon thread. Fixed the conjunctival flap to the surrounding conjunctiva with sutures, and covered the sclera with the surrounding bulbar conjunctiva.

Procedure: Autologous conjunctival transplantation in pterygium

PRF membrane transplantation in trabeculectomy for glaucoma

EXPERIMENTAL

The surgical procedure involved the creation of a scleral flap and conjunctiva in the usual manner. The subflap tissue was rinsed with balanced saline and then a small piece of tissue (measuring 1.5mm x 2mm) was removed from the inferior trabecular tissue of the scleral flap. In the corresponding position, peripheral iris excision was performed and the iris was rinsed to remove lost pigment in the vicinity of the incision. Once the orientation was verified, the PRF membrane was placed under the scleral flap.

Procedure: autologous PRF membrane grafting in trabeculectomy for glaucoma

Amniotic membrane in trabeculectomy for glaucoma

ACTIVE COMPARATOR

The surgical procedure began with creating the scleral flap and conjunctiva in the usual manner. The sub flap tissue was then rinsed with balanced saline, and a piece of tissue measuring 1.5mm x 2mm was excised from the inferior trabecular tissue of the scleral flap. Next, peripheral iris excision was performed in the corresponding position and the iris was rinsed to remove pigment in the vicinity of the incision. To control the tension of the sutures, the amniotic membrane was placed under the scleral flap, followed by meticulous suturing of the conjunctival flap.

Procedure: Amniotic membrane in trabeculectomy for glaucoma

PRF membrane transplantation in corneal ulcer

EXPERIMENTAL

The necrotic tissue of the corneal ulcer was cleared to expose the local fresh tissue, and the PRF group prepared PRF membrane and covered the surface of the test eye, and the autologous PRF membrane was continuously sutured to the corresponding surrounding tissues using 10-0 absorbable sutures so that the PRF membrane covered the entire portion of the lesion and was able to be anchored to it.

Procedure: PRF membrane grafting incorneal ulcer

Amniotic membrane in corneal ulcer

ACTIVE COMPARATOR

The necrotic tissue of the corneal ulcer was removed to reveal the fresh tissue in the area. After that, the excess amniotic membrane was carefully extracted and placed over the affected eye's surface. The membrane was then attached securely to the surrounding tissue using 10-0 absorbable sutures, covering the entire lesion and holding it in place for proper healing.

Procedure: Amniotic membrane in corneal ulcer

Interventions

A specially formulated PRF membrane, as described previously, was filled into the macular hole to promote fissure repair.

PRF membrane in macular hole

The treatment of the macular hole was ILM peeling.

Internal limmiting membrane(ILM) peeling in macular hole

Used of autologous PRF membrane to cover the exposed conjunctiva after pterygium excision.

PRF membrane transplantation in pterygium

Used of autologous conjunctiva to cover exposed sclera after pterygium excision

Autologous conjunctival transplantation in pterygium

Used of autologous PRF membranes to cover the exposed sclera after trabeculectomy for glaucoma.

PRF membrane transplantation in trabeculectomy for glaucoma

Used of amniotic to cover the exposed sclera after trabeculectomy for glaucoma.

Amniotic membrane in trabeculectomy for glaucoma

After surgical debridement of corneal ulcers, autologous PRF membrane was placed over the corneal wound to promote corneal healing

PRF membrane transplantation in corneal ulcer

After surgical debridement of corneal ulcers, autologous amniotic membrane was placed over the corneal wound to promote corneal healing

Amniotic membrane in corneal ulcer

Eligibility Criteria

Age20 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Diagnosis of macular hole confirmed by fundus examination;
  • Diagnosis of pterygium by slit lamp;
  • Patients requiring trabeculectomy for glaucoma;
  • Diagnosis of corneal ulcer confirmed by slit lamp.

You may not qualify if:

  • Combination of other active ophthalmic diseases, such as acute conjunctivitis and uveitis;
  • Previous history of ophthalmic trauma and ophthalmic surgery;
  • Recent use of anticoagulant or antiplatelet drugs;
  • Combination of serious systemic diseases such as hypertension and diabetes mellitus.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Eye Center, Renmin Hospital of Wuhan University

Wuhan, Hubei, 430060, China

Location

Related Publications (3)

  • Yang N, Xing Y, Zhao Q, Zeng S, Yang J, Du L. Application of platelet-rich fibrin grafts following pterygium excision. Int J Clin Pract. 2021 Oct;75(10):e14560. doi: 10.1111/ijcp.14560. Epub 2021 Jul 5.

    PMID: 34155746BACKGROUND
  • Yang N, Zeng S, Yang J, Lu G, Du L. Application of Platelet-Rich Fibrin Transplantation for Large Macular Hole. Curr Eye Res. 2022 May;47(5):770-776. doi: 10.1080/02713683.2022.2029906. Epub 2022 Mar 22.

  • Lu G, Zeng S, Huang R, Du L. Platelet-rich Fibrin Membrane Transplantation for the Treatment of Highly Myopic Macular Hole Retinal Detachment. Ophthalmol Ther. 2024 Sep;13(9):2425-2443. doi: 10.1007/s40123-024-00997-w. Epub 2024 Jul 26.

MeSH Terms

Conditions

Retinal PerforationsPterygiumGlaucomaCorneal Ulcer

Interventions

Trabeculectomy

Condition Hierarchy (Ancestors)

Retinal DiseasesEye DiseasesConjunctival DiseasesOcular HypertensionEye InfectionsInfectionsKeratitisCorneal Diseases

Intervention Hierarchy (Ancestors)

Filtering SurgeryOphthalmologic Surgical ProceduresSurgical Procedures, Operative

Study Officials

  • Lei Du

    Renmin Hospital of Wuhan University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
deputy chief physician

Study Record Dates

First Submitted

December 11, 2023

First Posted

January 11, 2024

Study Start

January 1, 2023

Primary Completion

June 30, 2025

Study Completion

December 31, 2025

Last Updated

January 12, 2024

Record last verified: 2024-01

Data Sharing

IPD Sharing
Will not share

This is a new technology and the information may be of commercial value to healthcare organisations and pharmaceutical companies. If this data is made public, it may result in other organisations or businesses gaining access to this information, which may affect the organisation's competitive advantage.

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