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Full Thickness Macular HoleNCT05828251

Full Thickness Macular Hole; Should it be Handled Subacutely?

A study testing Vitrectomy (Sequential phakoemulsification and vitrectomy), Combined phako-vitrectomy and Phako (Sequential phakoemulsification and vitrectomy) in people with Full Thickness Macular Hole, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.

Recruiting

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

Sites and contacts
Official record
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Trial summary

Full thickness macular hole, FTMH, is a retinal disease involving the fovea that cause central vision loss, metamorphopsia and central scotoma. The most effective treatment for FTMH is a pars plana vitrectomy and a tamponade with expansile gas. It is well known that vitrectomy accelerates cataract development. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Full Thickness Macular Hole
What is being tested?
Vitrectomy (Sequential phakoemulsification and vitrectomy), Combined phako-vitrectomy and Phako (Sequential phakoemulsification and vitrectomy)
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
56 participants
Where
1 siteDenmark
Study dates
30 Apr 2023to 1 Apr 2028
Phase
Interventional
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Idiopathic full thickness macular hole
  • Duration of symptoms of <30 days for Group 1 and 2
  • Duration of symptoms of 3-12 months for Group 3
  • FTMH size <400µm
  • >18 years
  • Able to give informed consent
  • Compliance for postoperative positioning

Who cannot join

  • High myopia (≤-3)
  • Traumatic macular hole
  • Prior ocular surgery, including cataract surgery
  • Other ocular diseases compromising the visual acuity (i.e., AMD, diabetic retinopathy, previous vein occlusion)
  • Posterior vitreous detachment (Weiss ring)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Denmark1 site, 1 recruiting
  • Rigshospitalet, Denmark

    Glostrup Municipality, Copenhagen, 2600

    Morten Dornonville de la Cour, MD, Prof.

    Recruiting

Other trials in Denmark

About this study

Full thickness macular hole, FTMH, is a retinal disease involving the fovea that cause central vision loss, metamorphopsia and central scotoma. The most effective treatment for FTMH is a pars plana vitrectomy and a tamponade with expansile gas. It is well known that vitrectomy accelerates cataract development. Vitrectomy can therefore be combined with cataract surgery in the same setting, a procedure that is shown to be safe, although increased inflammation and rates of central macular edema have been reported in some studies. Cataract surgery can also be performed prior or deferred until compromising the visual acuity after vitrectomy. Cataract-surgeries are more challenging in vitrectomized eyes due to lack of vitreous support and risk of loose zonules. The normal practice for FTMH at our department is therefore cataract surgery followed by vitrectomy 4 weeks later. A combined phaco-vitrectomy procedure is offered to patients who are at the labor market or when general anesthesia is required for the surgery. In non-presbyopic patients (<50 years) only vitrectomy is performed.

The visual improvement after surgery seems to be dependent on preoperative characteristics, such as the preoperative visual acuity, size of the hole and the duration of symptoms. The duration of symptoms is a known prognostic factor, and recently shown that the longer duration, the worse visual outcome. The precise timeframe for the optimal final outcome is not known.

Read more

The combined surgery is known to be safe in the treatment for epiretinal membrane, where a intravitreal gasfill is not necessary. However, the use of gas in FTHM surgery causes risk of increased movement of the newly inserted intraocular lens. This can lead to increased anterior segment inflammation with ensuing vision threatening cystic macular edema, as mentioned above.

The purpose of this study is to investigate whether small FTMH with a short duration of symptoms have better visual outcome with a prompt combined phako-vitrectomy (within two weeks), compared to the current standard of care of receiving cataract surgery as soon as possible and vitrectomy 4 weeks later. How the delay of surgery affects the visual outcome will also be investigated, by including patients with longer duration of symptoms. The main hypothesis is that the chance of better visual outcome is higher for macular holes with early surgery compared to the current standard of care and that the duration of symptoms has significant impact on the visual outcome.

Method

The study consists of 2 parts.

  1. Patients with idiopathic FTMH <400µm in diameter (as defined by The international vitreomacular traction study group classification), with a duration of symptoms of less than 30 days will be randomized into 2 groups: Group1: Combined phaco-vitrectomy within 2 weeks (after referral). Group 2: Current standard of care with cataract surgery as soon as possible and vitrectomy 4 weeks later.
  2. Group 3: Patients with small holes <400µm, with a duration of symptoms of more than 3 months and less than one year will be included in this part of the study. These patients will be treated and followed as in Group 2.

They will be reviewed a total of 7 times in Group 1 and 9 times in Group 2 and 3: a preoperative examination followed by 6/8 postoperative examinations. Additional examinations will be scheduled if needed.

Being tested
Vitrectomy (Sequential phakoemulsification and vitrectomy), Combined phako-vitrectomy, Phako (Sequential phakoemulsification and vitrectomy)
Keywords
Phako, Vitrectomy, Phako-vitrectomy, FTMH

What participants receive

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

  • Vitrectomy (Sequential phakoemulsification and vitrectomy)Procedure or surgery

    Standard treatment for FTMH at our department with phakoemulsification followed by pars plana vitrectomy and gas 4 weeks later.

  • Combined phako-vitrectomyProcedure or surgery

    Phakoemulsication and pars plana vitrectomy are performed in the same setting. This procedure is normally only offeres to selected cases at our department.

  • Phako (Sequential phakoemulsification and vitrectomy)Procedure or surgery

    Standard treatment for FTMH at our department with phakoemulsification followed by pars plana vitrectomy and gas 4 weeks later.

Study groups in NCT05828251
Study groupRoleWhat they receive
Combined Phako-Vitrectomy for FTMHExperimentalStudy 1: Patient randomized to this arm will receive a combined phako-vitrectomy within two weeks from referall day.
Receives: Procedure: Combined phako-vitrectomy
Sequential phako and vitrectomy for FTMHActive comparatorStudy 1: Patients randomized to this arm will receive a standard phacoemulsification as soon as possible. About four weeks after phacoemulsification a vitrectomy is performed.
Receives: Procedure: Vitrectomy (Sequential phakoemulsification and vitrectomy); Procedure: Phako (Sequential phakoemulsification and vitrectomy)
Longstanding FTMHOtherStudy 2: Patients with symptomduration of 3-12 months will be included in this part of the study in a prospective design.
Receives: Procedure: Vitrectomy (Sequential phakoemulsification and vitrectomy); Procedure: Phako (Sequential phakoemulsification and vitrectomy)

What is being measured

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

  1. Visual acuity

    Best corrected visual acuity measured with ETDRS, the ETDRS scoe will be converted to LogMAR

    Measured: 12 months after vitrectomy

Secondary outcomes (4)
  1. Metamorphopsia

    Measured by M-charts, for vertical and horisontal metamorfopisa. The M-charts consist of 19 dotted (dot size is 0.1°) lines with dot intervals ranging from 0.2° to 2.0° of visual angle.

    Measured: 12 months after vitrectomy

  2. Hole closure rates

    Either the hole closes og it doesn't.

    Measured: Measured 4 weeks after surgery

  3. Microperimetry

    Microperimetry is a procedure to assess retinal sensitivity while fundus is directly examined; it enables exact correlation between macular pathology and corresponding functional abnormality. Measured in mean retinal sensitivity (dB)

    Measured: 12 months after surgery

  4. Anterior chamber inflammation

    (FM). The FM is based on the measurement principle of laser light scattering detection. The instrument uses a diode laser beam to scan a measuring window that is projected inside the anterior chamber of the eye. As an aqueous protein (component of inflammation) passes through the focal point of the laser,light scattering occurs. The intensity of the scattered light (directly proportional to the amount of protein particles-flare) is detected by a photo-multiplier tube (PMT), which generates an electrical signal. This signal is immediately digitized to eliminate outside noise interference and are processed by a computer which displays the results for user analysis. The unit of measurement employed by the FM is "Photon Count" per millisecond.

    Measured: 1 day and 1 week after the first surgery

Timeline

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

  1. First posted25 Apr 2023
  2. Study start30 Apr 2023
  3. Primary completion1 Apr 2025 (estimated)
  4. Study completion1 Apr 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 N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized controlled trial in the first part om of the study, 28 patients in each arm. Prospective study in second part of the study with 28 patients.
Masking
None (open label)
Enrolment
56 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05828251
Sponsor's protocol ID
Rigshospitalet-RS studie
Status last verified
Apr 2024
First submitted
22 Mar 2023
Last updated
16 Apr 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Vitrectomy (Sequential phakoemulsification and vitrectomy), Combined phako-vitrectomy and Phako (Sequential phakoemulsification and vitrectomy) in people with Full Thickness Macular Hole, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.

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 5 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 16 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. 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.

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 Asrin Rasul, MD (004522365420, asrin.rasul@regionh.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual acuity (time frame: 12 months after vitrectomy). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 16 Apr 2024.

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