The Use of Bevacizumab as a Modulator of Wound Healing Following Trabeculectomy Surgery

Glaucoma Clinical Trial

— RAFTS  

Official title:

The Use of Bevacizumab as a Modulator of Wound Healing Following Trabeculectomy Surgery: A Single Centre Randomised Controlled Phase III Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02767219
• Other study ID #: MATR1001
• Secondary ID: 2013-000395-15
• Status: Completed
• Phase: Phase 3
• Start date: May 2016
• Est. completion date: May 2019

Study information

• Verified date: August 2021
• Source: Moorfields Eye Hospital NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase III randomised controlled pilot study which aims to assess the effectiveness of the use of bevacizumab in patients who have undergone trabeculectomy surgery, which appear to be showing early signs of failure.

Description:

Pharmacological enhancement of trabeculectomy using Mitomycin C (MMC) has significantly improved success rates. Despite this, some patients still mount aggressive scarring responses post-operatively and require additional subconjunctival injections of antifibrotic agents, such as 5-Fluorouracil (5-FU) to reduce scar formation and reduce the likelihood of surgical failure. There is concern that these agents are potentially toxic and may result in side effects such as keratopathy (loss of corneal epithelium) and are also painful for the patient. For those patients that are showing clinical evidence of potential scar formation, a more predictable and less toxic modulator of wound healing is desirable.

Vascular endothelial growth factor (VEGF) has been associated with angiogenesis in numerous pathological situations, including tumor growth, proliferative retinopathy, and rheumatoid arthritis. VEGF is also thought to play a pivotal role in ocular wound healing. It mediates the signal transduction cascade leading to tenon's fibroblast migration and proliferation and collagen gel contraction at the site of surgery, as well as angiogenesis. VEGF also causes persistent vascular permeability and vasodilation at the level of existing microvessels. Vessels with increased permeability are typically tortuous and dilated and this is the clinical appearance within the conjunctiva, suggestive of future excessive wound healing and scar formation following trabeculectomy. Early interventions such as subconjunctival injections of 5-Fluorouracil (5-FU) are therefore often considered when these clinical findings are apparent, in order to modify the course of wound healing.

The investigators propose a pilot study looking at the effect of serial injections of bevacizumab (an anti-VEGF agent) on modifying the wound healing response in patients showing early signs of future failure, compared to 5-Fluorouracil (5-FU). The purpose of the pilot is to also gather outcome data and information relating to safety and recruitment with a view to powering a definitive study addressing this issue.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: May 2019
• Est. primary completion date: February 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

1. Age 18 to 85 years, inclusive

2. Patient must have undergone standard trabeculectomy augmented with Mitomycin C, within the past 4-6 weeks.

3. Patients who in the clinician's opinion are mounting an aggressive wound healing response and demonstrate objective increase in bleb vascularity (moderate or severe on MBGS). Bleb function still needs to be maintained in the clinicians opinion and flat, scarred blebs are not to be included.

Exclusion Criteria:

1. Unwilling or unable to give consent, unwilling to accept randomization, or unable to return for scheduled protocol visits.

2. Pregnant or nursing women.

3. A history of cardiovascular or cerebrovascular events in the previous 6 months, such as angina, arrhythmia, Transient Ischaemic Attack, strokes, myocardial infarction.

4. Uncontrolled hypertension defined as systolic blood pressure >160millimeters of mercury (mmHg) or diastolic blood pressure >90millimeters of mercury (mmHg)

5. Subject hypersensitive to bevacizumab, 5-Fluorouracil (5-FU), and Mitomycin-C (MMC) and its excipients

6. Failed trabeculectomy bleb

7. Persistent wound leak following trabeculectomy at the time of randomisation

The following exclusions apply to the study eye only (i.e. they may be present for the non study eye

8. No light perception.

9. Aphakia

10. Previous, or planned, ocular surgery: vitreo-retinal, conjunctival surgery, etc considered likely to interfere with trabeculectomy outcome

11. Complicated cataract surgery

12. Cataract surgery less than 6 months in duration

13. Secondary glaucoma, other than Pigment Dispersion Syndrome (PDS) and Pseudoexfoliative (PXF)

14. Ocular trauma within the past 3 months

15. Active iris neovascularization or active proliferative retinopathy.

16. Severe posterior blepharitis.

17. Unwilling to discontinue contact lens use after surgery.

18. Current or recent (<3months) use of bevacizumab into the study eye.

Related Conditions & MeSH terms

• Glaucoma

Intervention

Drug:
• bevacizumab
Patients will be randomised to study arms with a 1:1 ratio. Once randomised, Group 2 will receive a subconjunctival injection of bevacizumab and a subconjunctival injection of dexamethasone 3.3mg/ml. This will be given for 4 consecutive weeks from time of entry into trial.
• 5-fluorouracil
Patients will be randomised to study arms with a 1:1 ratio. Once randomised, Group 1 will receive a subconjunctival injection of 5-fluorouracil and a subconjunctival injection of dexamethasone 3.3mg/ml. This will be given as required for 4 consecutive weeks from time of entry into trial. This is current standard practice.
• Dexamethasone
Both intervention groups will be given a subconjunctival injection of dexamethasone at the time of injection of either bevacizumab or 5-fluorouracil

Locations

Country	Name	City	State
United Kingdom	Moorfields Eye Hospital, Clinical Research Facility	London

Sponsors (1)

Lead Sponsor	Collaborator
Moorfields Eye Hospital NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time taken to recruit 30 subjects (from start of study)		study start date to18 months
Primary	Proportion of patients who are eligible who agree to be randomized		study start date to 18 months
Primary	Proportion of patients who are lost to follow up or who withdraw from the study		Baseline to 36 months
Secondary	Intraocular pressure		Baseline to 18 months
Secondary	Bleb morphology (as determined by Moorfields Bleb Grading system)		Baseline to 18 months
Secondary	Number of additional postoperative interventions with 5-fluorouracil (5-FU) and subconjunctival dexamethasone, following the 4 week trial intervention period; bleb needling.		received between baseline and 18 months of follow up
Secondary	Time to failure		Baseline to 18 months
Secondary	Number of topical ocular hypotensive medications at 3 months and 18 months		3 months and 18 months
Secondary	The incidence of complications will be recorded:		Baseline to 18 months