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Study of genetic alterations in patients with Keratoconus using DNA sequencing technique dna

Study of genetic mutations in patients with Keratoconus in western central Brazil using reaction polymerase chain in real time

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-624vfv
Enrollment
Unknown
Registered
2016-03-01
Start date
2015-01-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Keratoconus, mutation, gene

Interventions

Group or experimental case:   60 keratoconus patients (confirmed by Orbscan) aged 18 to 40 years old with no other ophthalmic disease or previous surgery or systemic diseases. 5 ml of blood will be co
Genetics
G05.365.795

Sponsors

Universidade Federal de Goias
Lead Sponsor
Fundação Banco de Olhos
Collaborator

Eligibility

Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Volunteers between 18-40 years of age with keratoconus; without keratoconus; no surgery or previous eye diseases; absence of systemic diseases; who accept sign the consent form and clarification

Exclusion criteria

Exclusion criteria: volunteers under the age of 18 years and above 40 years; who did not accept to sign the consent form and enlightenment; with diseases or previous eye surgery; systemic diseases

Design outcomes

Primary

MeasureTime frame
It`s hoped the polymorphism of the gene VSX1, mir-184, DOCK9 in patients with keratoconus and not the phenotype expression in control patients;Observe VSX1 gene polymorphism, mir-184 and DOCK9 by qPCR technique for identifying DNA mutant alleles

Secondary

MeasureTime frame
It is expected that the polymorphism VSX1 genes, miR-184, DOCK9 is expressed in at least 5% of the population with keratoconus and is statistically significant compared to controls

Countries

Brazil

Contacts

Public ContactFrancisco Rodrigues

VER-exelencia em oftalmologia

fcow@gmail.com+55 (62) 30969696

Outcome results

None listed

Source: REBEC (via WHO ICTRP)