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Outcomes of Early surgery to clear out the bleeding in the Eye caused by Diabtetes

Outcomes of early vitrectomy for vitreous hemeorrhage secondary to proliferative diabetic retinopathy - A prospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044623
Enrollment
50
Registered
2022-08-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H00-H59- Diseases of the eye and adnexa

Interventions

Intervention1: Vitrectomy: Surgery for the treatment of vitreous haemorrhage caused by proliferative diabetic retinopathy Intervention2: Vitrectomy: Surgical clearance of vitreous haemorrhage cause by

Sponsors

Sankara eye hospital Guntur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years 2. Diagnosis of diabetes mellitus (type 1 or type 2).  3. Vitreous haemorrhage (VH) in a patient with Proliferative Diabetic Retinopathy (PDR) causing vision impairment of duration less than one month, for which intervention is deemed necessary. 4. Patients who are willing and able to undergo vitrectomy within 2 weeks of presentation. 5. Visual acuity ranging between PL and ETDRS logMAR 0.3 (Snellenâ??s equivalent of 20/40 or 6/12).

Exclusion criteria

Exclusion criteria: 1. Any condition that precludes the participant from undergoing elective vitrectomy surgery in the study(e.g., unstable medical status including chronic renal failure requiring dialysis, blood pressure > 180/110, cardiovascular disease, pregnancy or lactation). 2. Systemic anti-VEGF or pro-vascular endothelial growth factor treatment within 4 months, intravitreal anti-VEGF in the study eye within 2 months of current vitreous haemorrhage onset, or intraocular corticosteroid treatment in the study eye within 4 months of current vitreous haemorrhage onset. 3. Participation in an investigational trial within 30 days that involves any drug that has not received regulatory approval for the indication being studied.  4. Potential participant is expected to lose follow-ups due to various reasons. 5. Evidence of traction or rhegmatogenous retinal detachment involving or threatening the macula. If the density of the haemorrhage precludes a visual assessment on the clinical exam to confirm eligibility, then it is recommended that the assessment be performed with ultrasound as standard care. 6. Evidence of uncontrolled glaucoma. 7. History of major ocular surgery (including vitrectomy, cataract extraction, scleral buckle, any intraocular surgery, YAG capsulotomy etc.) within 4 months or major ocular surgery other than vitrectomy anticipated within the next 6 months in the study eye. 8. Aphakia. 9. The evidence of severe external ocular infection, including conjunctivitis, chalazion, or substantial blepharitis.

Design outcomes

Primary

MeasureTime frame
To record the visual acuity in patients undergoing early vitrectomy.Timepoint: 18 months

Secondary

MeasureTime frame
To assess the incidence of rebleeding after performing an early vitrectomy. To analyse the impact of early vitrectomy on the progression of PDR - the new areas of Neovascularisation of retina elsewhere (NVE) or Fibro Vascular Proliferation (FVP).Timepoint: 18 months

Countries

India

Contacts

Public ContactASHOK K

SANKARA EYE HOSPITAL

docmadhu76@gmail.com9491021899

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026