Primary Vitrectomy With Silicone Oil or SF6 for Rhegmatogenous Retinal Detachment

Sponsor
Cairo University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05377606
Collaborator
(none)
62
1
2
14.2
4.4

Study Details

Study Description

Brief Summary

Rhegmatogenous retinal detachment (RRD) is the separation of the neurosensory retina from the retinal pigment epithelium caused by the presence of a break that leads to the passage of fluid from the vitreous cavity into the potential subretinal space. It is a sight threatening disease, affecting largely people 50 years or older, with an annual incidence varying between 6.3 and 17.9 people per 100,000 population, and is unfortunately increasing. Although other surgical options do exist for the repair of primary RRD, pars plana vitrectomy (PPV) has clear advantages and is certainly effective in the treatment of these patients.

Several agents are used for intraocular tamponade following PPV for RRD. These agents are either silicone oil (SO) or gases like air, perfluoropropane (C3F8), sulfur hexafluoride (SF6), or perfluoroethane (C2F6).

In addition to the complications uniquely peculiar to using SO, research has found out that a reduction in retinal sensitivity on microperimetry was greater in SO tamponade in comparison with gas, as well as poorer visual outcome, microvasculature damage and affection of retinal layers including ganglion cell complex (GCC) in the SO group.

Even though many studies were done to compare between SO and intraocular gas tamponades with respect to many aspects, only one study compared the effects SO had on macular vasculature and anatomy in comparison with air and no study at all to date has compared the SO to SF6 gas in terms of retinal vascular changes, correlating them to thinning of GCC and macular sensitivity, which is precisely the main aim of the current study.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Pars plana vitrectomy with silicone oil
  • Procedure: Pars plana vitrectomy with SF6
N/A

Detailed Description

Rhegmatogenous retinal detachment (RRD) is the separation of the neurosensory retina from the retinal pigment epithelium (RPE) caused by the presence of a break that leads to the passage of fluid from the vitreous cavity into the potential subretinal space. It is a sight threatening disease, affecting largely people 50 years or older, with an annual incidence varying between 6.3 and 17.9 people per 100,000 population, and is unfortunately increasing. Although other surgical options do exist for the repair of primary RRD, viz. scleral buckling and pneumatic retinopexy, primary pars plana vitrectomy (PPV) has clear advantages and is certainly effective in the treatment of these patients, with a primary success rate of 85%, making it the leading management modality.

Several agents are used for intraocular tamponade following PPV for RRD, in order to provide surface tension across the retinal breaks thus preventing the ingress once more of fluid into the subretinal space, giving time for the permanent seal provided by the retinopexy done whether photocoagulation or cryopexy. These agents are either silicone oil (SO) or gases like air, perfluoropropane (C3F8), sulfur hexafluoride (SF6), or perfluoroethane (C2F6).

In addition to the complications uniquely peculiar to using SO, research has found out that a reduction in retinal sensitivity on microperimetry was greater in SO tamponade in comparison with gas, as well as poorer visual outcome, microvasculature damage and affection of retinal layers including ganglion cell complex (GCC) in the former group leading to the so-called Silicone Oil-Related Visual Loss (SORVL).

Even though many studies were done to compare between SO and intraocular gas tamponades with respect to many aspects, only one study by Zhou et al in 2020 compared the effects SO endotamponade had on macular vasculature and anatomy in comparison with sterilized air tamponade and no study at all to date has compared the SO to SF6 gas in terms of retinal vascular changes, correlating them to thinning of GCC and macular sensitivity, which is precisely the main aim of the current study.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
62 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Care Provider)
Masking Description:
Surgeon will be masked to the tamponading agent (silicone oil or gas) till the end of the operation when either agent will be injected.
Primary Purpose:
Treatment
Official Title:
Macular Perfusion and Sensitivity Following Silicone Oil Tamponade Versus SF6 Gas for Primary Rhegmatogenous Retinal Detachment
Actual Study Start Date :
Dec 23, 2021
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Silicone oil group

Primary pars plana vitrectomy will be performed and silicone oil will be used as the tamponading agent. For these patients, optical coherence tomography (OCT) and angiography (OCTA), along with microperimetry will be done 2 months after the primary surgery. Then they will be scheduled for silicone oil removal after 3 months from the time of primary surgery. Finally, the OCT, OCTA, and microperimetry will be repeated once more after 4 months from the vitrectomy (i.e. one month after the silicone oil removal).

Procedure: Pars plana vitrectomy with silicone oil
Silicone oil will be used at the end of primary vitrectomy. OCT, OCTA and microperimetry will be done 2 months later. Silicone oil will be removed at 3 months. Finally, the OCT, OCTA, and microperimetry will be repeated once more after 4 months from the vitrectomy.

Active Comparator: Sulfur hexafluoride (SF6) group

Primary pars plana vitrectomy will be performed and sulfur hexafluoride (SF6) will be used as the tamponading agent. For these patients, optical coherence tomography (OCT) and angiography (OCTA), along with microperimetry will be done 2 months and 4 months after the primary surgery.

Procedure: Pars plana vitrectomy with SF6
Sulfur hexafluoride (SF6) will be used at the end of primary vitrectomy. OCT, OCTA, and microperimetry will be done 2 months and 4 months after surgery.

Outcome Measures

Primary Outcome Measures

  1. Macular perfusion - FAZ [At 2 and 4 months following primary vitrectomy]

    Comparison of foveal avascular zone area between the different treatment arms as a measure of macular perfusion.

  2. Macular perfusion - SVP [At 2 and 4 months following primary vitrectomy]

    Comparison of superficial retinal capillary vascular density between the different treatment arms.

  3. Macular perfusion - DVP [At 2 and 4 months following primary vitrectomy]

    Comparison of deep retinal capillary vascular density between the different treatment arms.

Secondary Outcome Measures

  1. Macular sensitivity [At 2 and 4 months following primary vitrectomy]

    Comparison of macular sensitivity between the different treatment arms using macular microperimetry.

  2. Thickness of ganglion cell complex [At 2 and 4 months following primary vitrectomy]

    Comparison of the thickness of ganglion cell complex in microns between the different treatment arms using optical coherence tomography (OCT)

  3. Best corrected visual acuity [At 2 and 4 months following primary vitrectomy]

    Comparison of best corrected visual acuity between the different treatment arms using standard Snellen charts.

  4. Retinal reattachment rate [At 4 months following primary vitrectomy]

    Comparison of single-operation anatomical success (retinal reattachment) rate between the different treatment arms

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Primary rhegmatogenous retinal detachment
Exclusion Criteria:
  • Macula-on retinal detachment

  • Change of decision of type of endotamponade used intraoperatively

  • Giant retinal tear

  • Proliferative vitreoretinopathy worse than grade B

  • Recent lens surgery within the previous 3 months prior to presentation

  • Prior vitreoretinal surgery

  • Macular hole

  • Signs of epiretinal membrane

  • Diabetic retinopathy

  • Macular degeneration or other macular disorders

  • Inferior retinal breaks between 4 and 8 o'clock

  • History of uveitis

  • History of glaucoma

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Medicine, Cairo University Cairo Egypt 11956

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Mina S. Abdelmalak, MSc, Cairo University
  • Study Chair: Soheir M. Mahmoud, PhD, Cairo University
  • Study Director: Ahmed A. Abdel Kader, PhD, Cairo University
  • Study Director: Asmaa M. Shuaib, PhD, Cairo University
  • Study Director: Ayman G. Elnahry, PhD, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mina Safe Abdelmesih Abdelmalak, Assistant Lecturer, Cairo University
ClinicalTrials.gov Identifier:
NCT05377606
Other Study ID Numbers:
  • MD-187-2021
First Posted:
May 17, 2022
Last Update Posted:
May 17, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 17, 2022