AzTrials
AzTrials

Eye DiseasesPhase 3TIGERNCT04663750

Vitrectomy, Subretinal Tissue Plasminogen Activator (TPA) and Intravitreal Gas for Submacular Haemorrhage Secondary to Exudative (Wet) Age-related Macular Degeneration (TIGER).

A Phase 3 study testing Pars plana vitrectomy, Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12 and subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mls in people with Eye Diseases and Macular Degeneration, Wet, run by King's College Hospital NHS Trust at 42 sites in 7 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

The centre of the retina (macula) at the back of the eye contains cells that give us our central vision that we use for reading and recognising faces. These cells can be damaged by a disease called wet age-related macular degeneration (AMD), where new abnormal blood vessels grow through the macula and leak fluid. Read more about this study

Who is it for?
Ages 50 to 120 years
What is being tested?
Pars plana vitrectomy, Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12 and subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mls
Could I receive a placebo?
No, everyone receives an active treatment
How many people
210 participants
Where
42 sitesin 7 countries
Study dates
16 Apr 2021to Dec 2028
Phase
Phase 3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 to 120 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • General
  • Males or females aged at least 50 years
  • Study eye
  • SMH, comprising sub-neuroretinal haemorrhage with or without sub-RPE haemorrhage, that occurs secondary to treatment naïve, or previously treated exudative AMD, including choroidal neovascularisation (CNV), idiopathic polypoidal choroidal vasculopathy (IPCV) and retinal angiomatous proliferation (RAP).
  • SMH involving the foveal centre that measures at least 1 disc diameter in greatest linear dimension.
  • Sub-neuroretinal haemorrhage at least 125 microns thick, measured at the foveal centre using spectral-domain optical coherence tomography (SD-OCT).
  • BCVA between counting fingers and an Early Treatment of Diabetic Retinopathy Study (ETDRS) letter score of 70, inclusive.

Who cannot join

  • General
  • Serious allergy to fluorescein or indocyanine green (ICG).
  • Hypersensitivity to alteplase, gentamicin, arginine, phosphoric acid, polysorbate 80 or aflibercept.
  • Stroke, transient ischaemic attack or myocardial infarction within 6 months.
  • Participation in another interventional study within 12 weeks of enrolment or planned to occur during this study.
  • Women who are breast feeding, pregnant, or planning to become pregnant during the clinical trial. Any sexually active women of childbearing potential must agree continued abstinence from heterosexual intercourse or to use highly effective methods of birth control for the duration up to 12 weeks after administration of IMP or the last administration of aflibercept on the trial. Men must also agree to use a condom if their partner is of child bearing potential, even if they have had a successful vasectomy. Females of childbearing potential are females who have experienced menarche and are not surgically sterilised (e.g. hysterectomy or bilateral salpingectomy) or post-menopausal (defined as at least 1 year since last regular menstrual period). Highly effective methods of birth control are those with a failure rate of < 1% per year when employed consistently and correctly, eg. combined (oestrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation via oral, intravaginal, and transdermal routes; progestogen-only hormonal contraception associated with inhibition of ovulation via oral, injectable, implantable, intrauterine device (IUD), or intrauterine hormone-releasing system ( IUS); or vasectomised partner.
Show all 21Show fewer
  • International Normalised Ratio (INR) greater than 3.5, unless it is anticipated that the INR can be brought below this level prior to vitrectomy, balancing the systemic risks with those of intraocular haemorrhage*.
  • Unwilling, unable, or unlikely to return for scheduled follow-up for the duration of the trial.
  • Any other condition which, in the opinion of the investigator, would prevent the participant from granting informed consent or complying with the protocol, such as dementia, mental illness, or serious systemic medical disease.
  • Study eye
  • SMH that is known or estimated to have been present for longer than 15 days, as evidenced by history, pre-trial clinical documentation, or fundus appearance.
  • SMH due to eye disease other than exudative AMD.
  • Current active proliferative diabetic retinopathy.
  • Current intraocular inflammation.
  • Current ocular or periocular infection other than blepharitis.
  • Current or known former high myopia (>6 dioptres).
  • Aphakia.
  • Other current or pre-existing ocular conditions that, in the opinion of the Investigator, will preclude any improvement in BCVA following resolution of SMH, such as severe central macular atrophy or fibrosis, dense amblyopia, macular hole involving the fovea, or very poor BCVA prior to presentation with SMH (counting fingers or worse).
  • Inadequate pupillary dilation or significant media opacities, which will prevent adequate clinical evaluation of the posterior segment or fundus imaging.
  • Intraocular surgery within 12 weeks of enrolment except for uncomplicated cataract surgery, which is permitted within 8 weeks of enrolment.
  • Applies only to participants receiving warfarin.

Trial locations and contacts

42 sites in 7 countries. Contact the study team or a site near you to ask about taking part.

Riti Desai, M.Sc.,M.Phil. contact

0044 2032991297 ext. 31297

ritidesai@nhs.net

42 sites in 7 countries

United Kingdom26 sites, 24 recruiting
  • Belfast Health and Social Care Trust

    Belfast, BT9 7AB

    Noemi Lois

    Recruiting
  • University Hospitals Sussex NHS Trust

    Brighton

    Withdrawn
  • Bristol Eye Hospital

    Bristol, BS1 2LX

    Johannes Keller

    Recruiting
  • Kent & Canterbury Hospital (East Kent University)

    Canterbury, Kent, CT1 3 NG

    Yvonne Luo

    Recruiting
  • Mid and South Essex NHS Foundation Trust

    Chelmsford, Essex, CM1 7ET

    Raiji Koothoor

    Recruiting
  • The Princess Alexandra Eye Pavilion

    Edinburgh, Scotlan, EH3 9HA

    Manjit Mehat

    Recruiting
  • Royal Devon and Exeter Hospital

    Exeter

    Conor Ramsden

    Recruiting
  • Gartnavel General Hospital

    Glasgow

    Withdrawn
  • Hull Royal Infirmary

    Hull, Yorkshire, HU3 2JZ

    Abdallah Ellabban

    Recruiting
  • Leicester Royal Infirmary

    Leicester

    Somnath Banerjee

    Recruiting
  • Royal Liverpool University Hospital

    Liverpool, L7 8 XP

    Ruman Hussain

    Recruiting
  • King's College Hospital NHS Foundation Trust

    London, London, SE5 9RS

    Timothy L Jackson, PhD, FRCOphth, +44 20 3299 1297 ext. 31297

    Riti Desai, M.Sc, M.Phil, +44 20 3299 1297 ext. 31297, ritidesai@nhs.net

    Recruiting
  • Barts Health NHST trust - Whipps Cross University Hospital

    London, E11 1NR

    Hadi Zambarakji

    Recruiting
  • Moorfields Eye Hospital

    London, EC1V 2PD

    Louisa Wickham

    Recruiting
  • Imperial College Healthcare NHS Foundation Trust (The Western Eye Hospital)

    London, NW1 5QH

    Rahila Zakir

    Recruiting
  • Maidstone and Tunbridge Wells NHS Trust

    Maidstone, ME16 9QQ

    Luke Membrey

    Recruiting
  • Manchester Royal Eye Hospital

    Manchester

    Tsveta Ivanova

    Recruiting
  • James Cook University Hospital, (South Tees NHSFT)

    Middlesbrough

    Saad Ahmed

    Recruiting
  • Royal Victoria Infirmary

    Newcastle upon Tyne, NE1 4LP

    Roxane Hillier

    Recruiting
  • Nottingham University Hospitals

    Nottingham

    Alexander Foss

    Recruiting
  • Oxford University Hospitals NHS Foundation Trust

    Oxford, OX3 9DU

    Sher Aslam

    Recruiting
  • University Hospitals Plymouth NHST

    Plymouth

    Vasant Raman

    Recruiting
  • University Hospital Southampton NHS foundation Trust

    Southampton, SO16 6YD

    Bhaskar Gupta

    Recruiting
  • Sunderland Eye Infimary

    Sunderland, Tyne and Wear, SR2 9HP

    Jonathan Smith

    Recruiting
  • Torbay and South Devon NHS

    Torquay, TQ2 7AA

    Eddie Doyle

    Recruiting
  • New Cross Hosp, Royal Wolverhampton NHST

    Wolverhampton

    Kam Balaggan

    Recruiting

Other trials in United Kingdom

Germany8 sites, 8 recruiting
  • University of Bonn

    Bonn

    Kristina Pfau

    Recruiting
  • University Medical Center Hamburg Eppendorf

    Hamburg

    Martin Spitzer

    Recruiting
  • Eye Clinic Ludwigshafen

    Ludwigshafen

    Lars-Olof Hattenbach

    Recruiting
  • Ludwig Maximilians-University München

    München

    Siegfried Priglinger

    Recruiting
  • Augenzentrum am St. Franziskus-Hospital Münster

    Münster

    Albrecht Lommatzsch

    Recruiting
  • Knappschaft Kliniken Saar GmbH, Sulzbach

    Sulzbach

    Boris Stanzel

    Recruiting
  • Ulm University Hospital

    Ulm

    Armin Wolf

    Recruiting
  • University hospital of Würzburg

    Würzburg

    Jost Hillenkamp

    Recruiting

Other trials in Germany

Netherlands2 sites, 2 recruiting
  • RadboudUMC

    Nijmegen

    Niels Crama

    Recruiting
  • Rottherdam ophtalmic institute

    Rotterdam

    Saskia Van Romunde

    Recruiting

Other trials in Netherlands

Poland2 sites, 2 recruiting
  • Ophthalmology Clinic Jasne Błonia

    Lodz

    Zofia Anna Nawrocka

    Recruiting
  • Warsaw Ophthalmology Hospital

    Warsaw

    Agnieszka Nowosielska

    Recruiting

Other trials in Poland

Switzerland2 sites, 2 recruiting
  • University Hospital Bern

    Bern

    Martin Sebastian Zinkernagel

    Recruiting
  • Jules-Gonin Hospital

    Lausanne

    Stappler Theodor

    Recruiting

Other trials in Switzerland

Ireland1 site, 1 recruiting
  • The Institute of Eye Surgery

    Waterford

    Eugene Ng

    Recruiting

Other trials in Ireland

Spain1 site, 1 recruiting
  • Hospital Vall d'Hebron

    Barcelona

    Jose Garcia Arumí

    Recruiting

Other trials in Spain

About this study

Official title: Vitrectomy, Subretinal Tissue Plasminogen Activator and Intravitreal Gas for Submacular Haemorrhage Secondary to Exudative Age-Related Macular Degeneration (TIGER): a Phase 3, Pan-European, Two-group, Observer-masked, Superiority, Randomised Controlled Surgical Trial.

The centre of the retina (macula) at the back of the eye contains cells that give us our central vision that we use for reading and recognising faces. These cells can be damaged by a disease called wet age-related macular degeneration (AMD), where new abnormal blood vessels grow through the macula and leak fluid. This can affect vision. In some cases, wet AMD can also cause a bleed under the macula, known as a submacular haemorrhage (SMH), which can lead to marked and persistent loss of vision in the eye.

The current standard treatment for wet AMD is to give injections containing 'anti-VEGF' drugs into the eye. Anti-VEGF drugs reduce the leakage of fluid so that the macula can become dry again and sight can improve.

Read more

Anti-VEGFs are also the current standard of care for SMH, mainly because there is no licensed treatment for the SMH itself (patients with SMH were excluded from most wet AMD studies).

The purpose of this study therefore is to compare two treatments:

  1. Standard treatment for wet AMD (anti-VEGF injections).
  2. Standard treatment above plus surgery. This study will find out if having surgery alongside anti-VEGF injections can improve vision further over the current standard treatment of anti-VEGF injections alone.
Read the detailed description

SMH is a rare but devastating complication of wet AMD. Untreated, SMH typically leads to permanent and severe loss of vision, ranging from 6/30 (approximately 20% normal vision) to only being able to perceive light versus dark (no useful vision).

There are no large, published, randomised controlled trials (RCTs) evaluating treatments for SMH. Hence there is no widely-accepted treatment approach. Some patients are managed by observation, others with drugs (anti-VEGF) injected into the eye, others with eye surgery (vitrectomy, subretinal TPA, gas) and combinations thereof. From a regulatory perspective the standard treatment is with anti-VEGF injections alone, since these are licensed for the treatment of wet AMD (and there is no treatment licensed for SMH). This study will test the hypothesis that surgery with anti-VEGF injections for SMH due to wet AMD is superior to the current standard of treatment with anti-VEGF injections alone. The results will help guide future clinical practice to maximise the visual outcomes for patients with SMH. Most potential participants will present or be referred to the clinics of the investigators who provide routine care for wet AMD. Referrals may arise from research networks, family physicians, optometrists or ophthalmologists.

After confirming the diagnosis of SMH, informed consent will be obtained and potential participants will be asked to sign a consent form. Following this, baseline screening will occur, including a clinical examination and a series of vision tests to confirm eligibility to take part in the study.

Once successfully screened, each participant will be randomly allocated to one of the two study groups:

  1. Standard current treatment with anti-VEGF injections: participants will be given their first injection into the study eye at the screening/baseline visit, or otherwise within a few days. Following this, each participant will receive another injection at month 1, another at month 2 and thereafter one injection every two months until the end of the study (month 12). Anaesthetic eye drops will be given to numb the eye before each injection.
  2. Standard current treatment with anti-VEGF injections plus surgery: participants will be given their first injection into the study eye at the time of surgery and then all other injections as per the schedule above. During the surgery, the clear gel (vitreous) that fills the inside of the eye will be removed and a clot-busting drug (TPA) will be injected into the eye to help break up the blood clot. The inside of the eye will then be filled with gas to help push the dissolved clot away from the macula. Various options for anaesthetic will be discussed with each participant before surgery, including (i) local anaesthetic only, (ii) local anaesthetic with some sedation, to reduce any anxiety or (iii) general anaesthetic so the participant is asleep during the surgery. If the participant also has a cataract or is likely to develop one, the surgeon will discuss the option of having cataract surgery as part of the same operation.

After the surgery, participants will be asked to keep their heads forward, to enable the gas bubble to move the blood clot away from the macula. This should be done for 50 minutes out of every hour for the first five days. During the 10-minute breaks, participants will be encouraged to move around and be active. At night, participants will be asked to sleep on the side of the operated eye, i.e. with the operated eye lowest. The gas is expected to disappear from the eye around 4-8 weeks after surgery.

Participants who have had surgery will be instructed to return for follow up the day after surgery and also one week later. All participants will also have a clinical examination at 6 and 12 months that will include tests of their vision. They will also attend regularly for anti-VEGF injections: every month for the first three visits, then every two months until the study is completed at month 12.

Being tested
Pars plana vitrectomy, Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12, subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mls, Intravitreal 20% sulfahexafluoride (SF6) gas tamponade
Keywords
Macular Degeneration, Wet, Sub-Macular Hemorrhage
Medical subject headings
Eye Diseases, Wet Macular Degeneration

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pars plana vitrectomyProcedure or surgery

    Pars plana vitrectomy

  • Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12Drug

    Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12.

  • subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mlsDrug

    Also called Actilyse (Boehringer Ingelheim)

    Subretinal injection of recombinant TPA (Alteplase, Actilyse, Boehringer Ingelheim) up to a maximum of 25 micrograms in 0.2 mls.

  • Intravitreal 20% sulfahexafluoride (SF6) gas tamponadeDrug

    Intravitreal 20% sulfahexafluoride (SF6) gas tamponade.

Study groups in NCT04663750
Study groupRoleWhat they receive
Arm A - Surgery with afliberceptExperimentalSurgery with aflibercept at the end of surgery, with post-operative review day 1 and week 1 (day 7)
Receives: Procedure: Pars plana vitrectomy; Drug: Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12; Drug: subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mls; Drug: Intravitreal 20% sulfahexafluoride (SF6) gas tamponade
Arm B - Aflibercept monotherapyActive comparatorAflibercept monotherapy commencing at baseline.
Receives: Drug: Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. assessment of Early Treat of Diabetic Retinopathy Study (ETDRS) letters of best-corrected visual acuity (BCVA) in the study eye.

    The primary outcome is the proportion of participants with a BCVA gain ≥10 ETDRS letters in the study eye at the 12 month visit.

    Measured: 12 months

Secondary outcomes (7)
  1. Assessment of Early Treatment Diabetic Retinopathy Study (ETDRS) letter improvement in Best-Corrected Visual Acuity (BCVA) in the study eye

    Change in ETDRS letters in BCVA in the study eye at the month 6 visit.

    Measured: 6 months

  2. Mean ETDRS BCVA

    Measured: 6 and 12 months

  3. Radner maximum reading speed

    Measured: 6 and 12 months

  4. Area of scotoma size using Humphrey Field Analyser 10-2 or equivalent

    Measured: 6 and 12 month

  5. National Eye Institute 25-item visual function questionnaire (NEI VFQ-25). composite score.

    Measured: 6 and 12 months.

  6. EQ-5D-5L with vision bolt-on score.

    Measured: 6 and 12 months.

  7. Presence/absence of subfoveal fibrosis and/or atrophy and area of fibrosis/atrophy using multimodal reading centre image analysis.

    Presence or absence of subfoveal fibrosis and/or atrophy and area of fovea-involving fibrosis/atrophy assessed using multimodal imaging by an independent reading centre, combining spectral domain optical coherence tomography (SD-OCT), fundus autofluorescence (FAF) and stereo fundus photographs.

    Measured: 12 months.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Dec 2020
  2. Study start16 Apr 2021
  3. Primary completionDec 2028 (estimated)
  4. Study completionDec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Experimental arm: pars plana vitrectomy, sub retinal injection of recombinant tissue plasminogen activator (TPA), intravitreal sulfahexafluoride (SF6) gas tamponade and intravitreal aflibercept. Active comparator arm: intravitreal aflibercept.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
210 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04663750
Sponsor's protocol ID
IRAS Project ID: 276366
Other IDs
2020-004917-10
Acronym
TIGER
Status last verified
Jul 2026
First submitted
27 Nov 2020
Last updated
11 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Lee CN, Desai R, Ramazzotto L, Wafa H, Wang Y, Bunce C, Doungsong K, Ezeofor V, Edwards RT, Lois N, Steel DH, Peto T, Hillenkamp J, van Meurs JC, Reeves BC, Jackson TL. Vitrectomy, subretinal Tissue plasminogen activator and Intravitreal Gas for submacular haemorrhage secondary to Exudative Age-Related macular degeneration (TIGER): update to study protocol and addition of a statistical analysis plan and health economic analysis plan for a randomised controlled surgical trial. Trials. 2025 Apr 14;26(1):131. doi: 10.1186/s13063-025-08727-8.

    PubMed 40229856
  • Jackson TL, Bunce C, Desai R, Hillenkamp J, Lee CN, Lois N, Peto T, Reeves BC, Steel DH, Edwards RT, van Meurs JC, Wafa H, Wang Y. Vitrectomy, subretinal Tissue plasminogen activator and Intravitreal Gas for submacular haemorrhage secondary to Exudative Age-Related macular degeneration (TIGER): study protocol for a phase 3, pan-European, two-group, non-commercial, active-control, observer-masked, superiority, randomised controlled surgical trial. Trials. 2022 Jan 31;23(1):99. doi: 10.1186/s13063-021-05966-3.

    PubMed 35101110

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Pars plana vitrectomy, Intravitreal 2 mg aflibercept will be injected at baseline then monthly for two further doses, then 2-monthly until month 12 and subretinal injection of recombinant TPA (Alteplase) up to a maximum of 25 micrograms in 0.2 mls in people with Eye Diseases and Macular Degeneration, Wet, run by King's College Hospital NHS Trust at 42 sites in 7 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 21 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 11 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 42 sites in United Kingdom, Germany, Netherlands, Poland, Switzerland and 2 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Riti Desai, M.Sc.,M.Phil. (0044 2032991297 ext. 31297, ritidesai@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

assessment of Early Treat of Diabetic Retinopathy Study (ETDRS) letters of best-corrected visual acuity (BCVA) in the study eye. (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04663750, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2026.

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