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Rubinstein-Taybi syndrome and keloids

Rubinstein-Taybi syndrome and keloids - Rubinstein-Taybi syndrome and keloids

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38183
Enrollment
25
Registered
2012-01-10
Start date
2012-04-02
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

itching scar keloid

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with the Rubinstein Taybi syndrome Patients with keloids Age 18 years or above Written informed consent For the biopsy study: the patient needs general anaesthesia for a planned intervention for patient care reasons

Exclusion criteria

Exclusion criteria: Insufficient understanding of the purpose of the study by parents / other legal representative Age

Design outcomes

Primary

MeasureTime frame
The clinical characteristics of keloids The histological characteristics of keloids The moleculair and cell-biological characteristics of keloids in RTS, mainly the TGF beta pathway and HAT function

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)