- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT06601101
Effekter av aktuell insulin på hornhinneepitelheling etter korneal kryssbinding hos pasienter med keratokonus
Effekter av aktuell insulin på korneal epitelheling etter korneal kryssbinding hos pasienter med keratokonus: en randomisert klinisk studie
The cornea plays a fundamental role in vision, being a complex tissue essential for ocular health. In ophthalmological practice, there are situations such as corneal crosslinking, where damage to the corneal epithelium occurs. Crosslinking is a surgical procedure aimed at strengthening collagen bonds in the corneal stroma to prevent the progression of keratoconus, through the application of topical riboflavin followed by ultraviolet (UV-A) radiation. To enhance the effectiveness of riboflavin and UV-A radiation, the corneal epithelium needs to be removed, which can cause postoperative pain and discomfort, as well as increase the risk of complications such as infections, scarring, corneal opacities, perforations, and recurrent epithelial erosions. Several growth factors play a role in epithelial healing, and the discovery of insulin in the tear film and the presence of insulin and Insulin-Like Growth Factor (IGF-1) receptors in the cornea has raised the hypothesis that insulin may modulate the cornea's wound healing response. Since then, topical insulin has been used for various ocular pathologies, including dry eye disease, persistent epithelial defects, and neurotrophic ulcers. Based on this knowledge, studies have been developed, and promising results regarding the use of insulin in corneal healing have been reported, providing a scientific foundation for the realization of this project.
The objective of this study was to evaluate the effect of insulin eye drops at a concentration of 50 IU/ml on epithelial healing in non-diabetic patients undergoing epithelial debridement for corneal crosslinking. To this end, a randomized, double-masked clinical trial was conducted with two groups, one being the control group, in which researchers compared the epithelial healing rate in mm²/h between the insulin group and the placebo group, as the primary outcome. Patients diagnosed with keratoconus and with an indication for the crosslinking procedure were invited to participate.
The study was designed to assess and quantify the impact of topical insulin on epithelial defect closure in patients undergoing crosslinking, compared to placebo.
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
Patients from the Keratoconus Clinic of the Hospital de Clínicas, State University of Campinas (UNICAMP), Brazil, with a diagnosis of keratoconus and an indication for corneal crosslinking were evaluated with visual acuity, refraction, slit-lamp biomicroscopy, Goldmann applanation tonometry, corneal specular microscopy (EM-3000, Tomey) for endothelial cell count, and corneal tomography (Pentacam HR, Oculus).
Eligible patients who signed the informed consent form (with the legal guardian also signing for participants younger than 18 years) underwent crosslinking. After the procedure, participants were allocated to two groups (insulin and placebo) by block randomization with blocks of four, stratified by sex. The random sequence was generated at random.org/lists and concealed in sealed opaque envelopes prepared by an independent assistant. Envelopes were opened sequentially at enrollment by investigators who did not take part in outcome assessment. One participant underwent crosslinking in both eyes, which were allocated to different groups; the eye was the unit of analysis.
Crosslinking was standardized for all participants and performed by third-year ophthalmology residents supervised by attending physicians. Central 8.0-mm epithelial debridement was performed with an optical zone marker of the same diameter: 30% alcohol was applied within the marker for 10 seconds and dried with an ophthalmic sponge, and the epithelium was removed with a corneal scarifier spatula. Riboflavin 0.1% (400 mOsm) in a hydroxypropyl methylcellulose vehicle was used, with UVA irradiation at 9 mW/cm² for 10 minutes (fluence 5.4 J/cm²) using the Eyelink Crosslink device (Eyetec, São Carlos, Brazil). At the end of the procedure, the size and shape of the debrided area were checked with the 8.0-mm marker, and participants whose debridement did not meet this standard were excluded.
The insulin group received NPH insulin 50 IU/mL eye drops (Eye Pharma, São Paulo, Brazil) four times daily, and the placebo group received 0.5% methylcellulose eye drops (Eye Pharma), the vehicle of the insulin formulation, four times daily, until complete epithelial healing. The bottles were identical and were labeled on the prescription as "compounded eye drops". Participants and outcome assessors were masked to group allocation. Both groups received moxifloxacin 5 mg/mL every 6 hours (Oftalmox; Geolab), prednisolone acetate 10 mg/mL every 6 hours (Ster; União Química), 0.15% sodium hyaluronate every 4 hours (Hyabak; Laboratoires Théa) and a silicone hydrogel bandage contact lens (Air Optix plus HydraGlyde; Alcon) until complete epithelial healing. Moxifloxacin and the study eye drops were then discontinued, and prednisolone was tapered weekly until one month after the procedure.
Crosslinking was always performed on Tuesdays, and assessments took place 18, 42 and 66 hours after the procedure (postoperative days 1 to 3). If epithelialization was incomplete at 66 hours, a further visit was scheduled on postoperative day 6 and every 48 hours thereafter until complete epithelialization. At each visit, the epithelial defect was photographed with the Keratograph 5M (OCULUS) and slit-lamp biomicroscopy was performed. The defect area was measured with ImageJ software by an investigator masked to allocation and reviewed independently by a second masked investigator. Complete epithelial healing was defined as the absence of an epithelial defect after fluorescein instillation on Keratograph 5M images, confirmed by two examiners on slit-lamp examination.
The primary outcome is the corneal epithelialization rate (mm²/h). Secondary outcomes are time to complete epithelialization and adverse events, in addition to endothelial cell density. Later follow-up visits took place at 30 and 60 days after crosslinking.
Studietype
Registrering (Faktiske)
Fase
- Fase 3
Kontakter og plasseringer
Studiesteder
-
-
São Paulo
-
Campinas, São Paulo, Brasil, 13.083-887
- State University of Campinas
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Age 14 years or older
- Diagnosis of keratoconus with an indication for corneal crosslinking
Exclusion Criteria:
- Diabetes mellitus
- Dry eye disease
- Limbal stem cell deficiency
- Glaucoma
- Allergy to insulin or methylcellulose
- Irregular epithelial debridement and/or debridement other than 8.0 mm during the crosslinking procedure
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Insulin
NPH insulin 50 IU/mL eye drops (Eye Pharma, São Paulo, SP, Brazil), one drop four times daily until complete corneal epithelialization, added to the standard postoperative regimen. |
Insulin eye drops in the postoperative prescription for corneal crosslinking
Andre navn:
|
|
Placebo komparator: Placebo
0.5% methylcellulose eye drops (Eye Pharma, São Paulo, SP, Brazil), the vehicle of the insulin formulation, one drop four times daily until complete corneal epithelialization, added to the standard postoperative regimen. |
Placebo eye drops of 0.5% Methylcellulose in the postoperative prescription for corneal crosslinking
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Corneal Epithelial Healing Rate
Tidsramme: From crosslinking until complete epithelialization, assessed at 18, 42 and 66 hours, on day 6 and every 48 hours thereafter.
|
Rate of corneal re-epithelialization (mm²/h), calculated as the epithelial defect area at the first postoperative assessment (18 hours) divided by the time elapsed until complete epithelialization. Defect area measured on Keratograph 5M (OCULUS) images with ImageJ software by masked investigators. |
From crosslinking until complete epithelialization, assessed at 18, 42 and 66 hours, on day 6 and every 48 hours thereafter.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Endothelial cell count
Tidsramme: 60 days
|
Endothelial cell count loss in each group, if any |
60 days
|
|
Incidence of corneal haze
Tidsramme: 60 days.
|
Incidence of corneal haze in each group. |
60 days.
|
|
Time to complete epithelialization
Tidsramme: From crosslinking until complete epithelialization.
|
Time (hours) from crosslinking to the first assessment at which complete epithelial closure was documented (absence of an epithelial defect after fluorescein instillation on Keratograph 5M images, confirmed on slit-lamp examination). Closure could only be ascertained at scheduled visits. |
From crosslinking until complete epithelialization.
|
|
Adverse events
Tidsramme: From crosslinking until the end of follow-up.
|
Number of eyes with ocular adverse events (e.g., infectious keratitis, sterile infiltrates, persistent epithelial defect, allergic reaction to study eye drops) recorded at each study visit. |
From crosslinking until the end of follow-up.
|
Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Epithelial Defect Area
Tidsramme: 18, 42 and 66 hours after crosslinking.
|
Area of the corneal epithelial defect (mm²) measured on Keratograph 5M images with ImageJ software. |
18, 42 and 66 hours after crosslinking.
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Studiestol: Monica Alves, PhD, State University of Campinas (Unicamp)
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Øyesykdommer
- Keratokonus
- Korneal sykdommer
- Hormoner
- Hormoner, hormonsubstitutter og hormonantagonister
- Farmasøytiske løsninger
- Peptidhormoner
- Peptider
- Aminosyrer, peptider og proteiner
- Farmasøytiske preparater
- Farmakologiske handlinger
- Kjemiske handlinger og bruk
- Terapeutisk bruk
- Løsninger
- Spesialbruk av kjemikalier
- Insulin, langtidsvirkende
- Insuliner
- Pankreashormoner
- Proinsulin
- Insulin
- Oftalmiske løsninger
- Insulin, isofan
Andre studie-ID-numre
- 77229224.8.0000.5404
- Topical Insulin (Annen identifikator: Unicamp)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
The de-identified dataset analyzed during the current study is available from the corresponding author on reasonable request.
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