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Umbilical cord grafting in corneal reconstruction

Outcome of Umbilical Cord Patch grafting in corneal reconstruction in cases of descemetocele and corneal perforations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/043735
Enrollment
34
Registered
2022-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: H178- Other corneal scars and opacities

Interventions

Intervention1: Umbilical Cord Patch: Dried Umbilical cord patch will be trimmed according to the size of the corneal defect, and placed over the corneal defect as a graft and will be sutured with 8 to

Sponsors

Regional Institute of Ophthalmology Kolkata
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subject with a known case of corneal perforation and descemetocele due to both infectious and non - infectious cause 2. Subjects with corneal perforation due to trauma 3. Subjects with corneal perforation size between 3.5 to 5.5 mm in diameter 4. Patients with no previous history of keratoplasty 5. In case of bilateral cases, the severely affected eye is included 6. Patients who are willing to sign the informed consent

Exclusion criteria

Exclusion criteria: 1. Corneal perforation 2. Any active corneal infection 3. Corneal scar not easily distinguishable from a current ulcer. 4. Previous penetrating keratoplasty in the affected eye. 5. 6. Pregnancy (by history or urine test) or breast-feeding. 7. Acuity worse than 6/60 (20/200) in the other eye. 8. Known allergy to medications (antibiotics or preservatives). 9. No light perception in the affected eye 10. Patients who are not willing to sign the consent form

Design outcomes

Primary

MeasureTime frame
Graft host integration and thickness of corneaTimepoint: 1 month, 3 month, 6 month

Secondary

MeasureTime frame
AC depthTimepoint: 1month, 3month, 6 month;Improvement of visual acuityTimepoint: 1month, 3 months, 6 months;Inflammatory reactionsTimepoint: 1 month, 3 month, 6 month;Measurement of IOPTimepoint: 1 month, 3month, 6 month;Re epithelialisationTimepoint: 1 month

Countries

India

Contacts

Public ContactJayanta Dutta

Deben Mahato Government Medical College & Hospital, Purulia

docjayantadutta@rediffmail.com9433571337

Outcome results

None listed

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