Use of digital and conventional feeding plates created for patients with cleft lip and palate and cleft palate

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033346

Enrollment

Registered

2024-01-19

Start date

2024-02-15

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Q35-Q37

Interventions

Group 1: Group 1: Feeding plate conventionally molded and manufactured Group 2: Group 2: Feeding plate digitally molded and manufactured

Eligibility

Sex/Gender

All

Age

0 Years to 18 Months

Inclusion criteria

Inclusion criteria: cleft palate

Exclusion criteria

Exclusion criteria: Syndromic disorders

Design outcomes

Primary

Measure	Time frame
Are digitally molded and manufactured feeding plates equivalent to conventionally molded and manufactured drinking plates in terms of wearing comfort, type and duration of impression and production? Outcome 1: Compares the impression and production, filling out a registration form with parameters for the production time is done on the day of production Outcome 2: Comfort and fastening, evaluated by parents using a questionnaire, the test period is 20 days	—

Measure

Time frame

Are digitally molded and manufactured feeding plates equivalent to conventionally molded and manufactured drinking plates in terms of wearing comfort, type and duration of impression and production? Outcome 1: Compares the impression and production, filling out a registration form with parameters for the production time is done on the day of production Outcome 2: Comfort and fastening, evaluated by parents using a questionnaire, the test period is 20 days

—

Secondary

Measure	Time frame
Can the digital method prevent the risks of conventional impression making (e.g. aspiration of impression material)? Outcome: statistical evaluation: Does digital production meet the gold standard?, evaluation of the collected data on the basis of registration forms and questionnaires after the study has been completed and the inclusion of all subjects	—

Countries

Germany

Contacts

Public ContactKatharina Schaffrath

Uniklinik RWTH Aachen

kaschaffrath@ukaachen.de004924136882

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026