Measuring the Volumes of Hypertrophic Scars and Keloids, Two Specific Kind of Scars, Over Different Points in Time in Patients Who Have Undergone Surgery and Evaluate 3D-cameras As a Possible Measuring and Documenting Tool Including Volumetry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: 3D-Pictures.
- Who it may be relevant to
- Registry conditions: Keloid Scar Following Surgery, Scars, Hypertrophic, Scar Keloid. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Switzerland
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Quantification of Hypertrophic Scar Tissue or Keloid Using a 3D-Camera
Overview
Measuring the volumes of hypertrophic scars and keloids, two specific kind of scars, over different points in time in patients who have undergone surgery and evaluate 3D-cameras as a possible measuring and documenting tool including volumetry.
Detailed description
The objective of this study is to utilize a 3D camera to measure the volumes of hypertrophic scars and keloids in patients at specified time points. The time points for measurement include day 0, as well as 3, 6, and 12 months. The 3D camera will be evaluated for their efficacy in measuring and documenting the volumes of the scars. This evaluation will include volumetry, which is the measurement of the three-dimensional space occupied by an object.
Interventions
- Other 3D-Pictures
3D-Pictures will be taken of hypertrophic scars and keloids to document them.
Primary outcome measures
- Measurability [Time frame: Day 0, Month 3, 6 and 12]
Eligibility criteria
Inclusion criteria
- All patients with hypertrophic scars or keloids, written consent to participate in the study, minimum age of 18 years.
Exclusion criteria
- Absence of written consent, unwillingness to contribute data, inability to understand the study protocol.
- lack of hypertrophic scars or keloid
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
Switzerland · 1 center
- Universitätsspital Zürich — Zurich
Identifiers
NCT: NCT06806735 · 2024-01147