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Effectiveness of Ottobock Helmet Therapy in Infants With Plagiocephaly, Brachycephaly or Combination of Both

Effectiveness of Ottobock Helmet Therapy in Infants With Plagiocephaly, Brachycephaly or Combination of Both and Parents' Satisfaction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05154175
Enrollment
452
Registered
2021-12-10
Start date
2021-11-15
Completion date
2022-01-31
Last updated
2022-04-12

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

Conditions

Brachycephaly, Plagiocephaly, Nonsynostotic, Plagiocephaly, Positional

Keywords

Cranial orthosis, Helmet treatment

Brief summary

The objective of the research is to measure the effectiveness of the Ottobock helmet, an innovative 3D-printed cranial orthosis used to correct infant cranial positional deformation: plagiocephaly, brachycephaly or combination of both. This research is a retrospective multi-centric study composed of a collection of clinical data from orthotists database and a survey for patient's parents.

Detailed description

The Ottobock helmet is a cranial orthosis used to correct infant cranial positional deformation: plagiocephaly, brachycephaly or combination of both. This medical device is a 3D-printed helmet, with an elastic closing system which allow the head growth, maintain a constant pressure in the helmet and ensure a good adjustment. Even though there is an effectiveness observed, there are no existing clinical evidences on this type of helmet so far, and there is a need to conduct a research on a large number of patients to measure the effectiveness and describe the population treated. This study will give more information to health professionals (doctors, orthopedic technicians, etc.) and health authorities, about the benefits of the orthopedic treatment of the positional cranial deformations in infants. The study is composed of an electronic case report form (eCRF) to be fulfilled by the orthotists and an electronic questionnaire (ePRO) to be fulfilled by the patient's parents. The electronic questionnaires, data treatment and analysis are handled by a Contract Research Organization (CRO).

Interventions

DEVICEOttobock helmet

Patients treated in current practice

Sponsors

Quanta Medical
CollaboratorINDUSTRY
Otto Bock France SNC
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Months to 2 Years
Healthy volunteers
No

Inclusion criteria

* Infant with positional cranial deformation * Infant treated with an Ottobock helmet between May 1st, 2020 and May 1st, 2021

Exclusion criteria

* Patient whose parents (or legal guardians) disagree to participate in the study. * Patient whose parents (or legal guardians) are unable to understand or answer the questionnaire.

Design outcomes

Primary

MeasureTime frameDescription
Cranial deformation index6 weeksThe cranial deformation index is a ratio (%) of head diameters characterizing head deformation.

Secondary

MeasureTime frameDescription
Satisfaction of parents regarding the device and the services provided by the orthotistThrough study completion, an average of 6 monthsQUEST 2.0

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026