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.
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
- Recruiting
Rigshospitalet, Denmark
Glostrup Municipality, Copenhagen, 2600
Morten Dornonville de la Cour, MD, Prof.
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.
- 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.
- 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.
- Conditions
- Full Thickness Macular Hole
- 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 group | Role | What they receive |
|---|---|---|
| Combined Phako-Vitrectomy for FTMH | Experimental | Study 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 FTMH | Active comparator | Study 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 FTMH | Other | Study 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.
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)
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
Hole closure rates
Either the hole closes og it doesn't.
Measured: Measured 4 weeks after surgery
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
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.
- First posted25 Apr 2023
- Study start30 Apr 2023
- Primary completion1 Apr 2025 (estimated)
- Study completion1 Apr 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Full Thickness Macular HoleStudies of the same condition, open and under way.
- More trials run by Copenhagen University Hospital, RigshospitaletThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Copenhagen University Hospital, Rigshospitalet
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Asrin Rasul, Copenhagen University Hospital, Rigshospitalet
- Investigators
- Morten Dornonville de la Cour, MD, Prof., Principal investigator, Copenhagen University Hospital, Rigshospitalet
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
Study at a glance
From the registry record, last updated by the sponsor on 16 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Full Thickness Macular Hole; Should it be Handled Subacutely?
- ClinicalTrials.gov ID
- NCT05828251
- Acronym / sponsor ID
- Rigshospitalet-RS studie
- Conditions
- Full Thickness Macular Hole
- Keywords
- Phako, Vitrectomy, Phako-vitrectomy, FTMH
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 56 participants (estimated)
- Lead sponsor
- Copenhagen University Hospital, RigshospitaletUniversity, hospital or other
- Study start
- 30 Apr 2023 (actual)
- Primary completion
- 1 Apr 2025 (estimated)
- Study completion
- 1 Apr 2028 (estimated)
- First posted
- 25 Apr 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
- 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.
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- 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.
| Arm | Type | Receives |
|---|---|---|
| Combined Phako-Vitrectomy for FTMH | Experimental | Procedure: Combined phako-vitrectomyStudy 1: Patient randomized to this arm will receive a combined phako-vitrectomy within two weeks from referall day. |
| Sequential phako and vitrectomy for FTMH | Active comparator | Procedure: Vitrectomy (Sequential phakoemulsification and vitrectomy), Procedure: Phako (Sequential phakoemulsification and vitrectomy)Study 1: Patients randomized to this arm will receive a standard phacoemulsification as soon as possible. About four weeks after phacoemulsification a vitrectomy is performed. |
| Longstanding FTMH | Other | Procedure: Vitrectomy (Sequential phakoemulsification and vitrectomy), Procedure: Phako (Sequential phakoemulsification and vitrectomy)Study 2: Patients with symptomduration of 3-12 months will be included in this part of the study in a prospective design. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- 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
Key exclusion criteria (5 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Vitrectomy (Sequential phakoemulsification and vitrectomy)Standard treatment for FTMH at our department with phakoemulsification followed by pars plana vitrectomy and gas 4 weeks later. | Procedure or surgery | Longstanding FTMH, Sequential phako and vitrectomy for FTMH |
| Combined phako-vitrectomyPhakoemulsication and pars plana vitrectomy are performed in the same setting. This procedure is normally only offeres to selected cases at our department. | Procedure or surgery | Combined Phako-Vitrectomy for FTMH |
| Phako (Sequential phakoemulsification and vitrectomy)Standard treatment for FTMH at our department with phakoemulsification followed by pars plana vitrectomy and gas 4 weeks later. | Procedure or surgery | Longstanding FTMH, Sequential phako and vitrectomy for FTMH |
Primary outcome
Visual acuity
Time frame: 12 months after vitrectomy
Best corrected visual acuity measured with ETDRS, the ETDRS scoe will be converted to LogMAR
4 secondary outcomes
Metamorphopsia
Time frame: 12 months after vitrectomy
Hole closure rates
Time frame: Measured 4 weeks after surgery
Microperimetry
Time frame: 12 months after surgery
Anterior chamber inflammation
Time frame: 1 day and 1 week after the first surgery
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Apr 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Morten Dornonville de la Cour, MD, Prof. principal investigator
Copenhagen University Hospital, Rigshospitalet
1 site in 1 country: see every site and its status.
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.