Clinical research for efficacy and safety of plastic surgery of the nose

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT1090220220

Enrollment

Registered

2015-08-03

Start date

2015-08-04

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Patient undergoing plastic surgery of the nose

Interventions

Intervention type:BEHAVIOUR Name of intervention:Test and observation Dose form / Japanese Medical Device Nomenclature:NOT APPLICABLE Route of administration / Site of application:NOT APPLICABLE Dose

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with plans to repair the nose deformation by plastic surgery of the nose 2. Patients can agree to the shooting and provision of roentgenographic cephalogram 3. Patients more older than 17 years of age (at the time of obtaining informed consent) 4. Patients themselves and their representative (in the case of a patient is less than 20 years of age) can understand the contents of the investigation, and be able to get a written informed consent

Exclusion criteria

Exclusion criteria: 1.Unsuitable patients as a target of investigation determined by medical doctor

Design outcomes

Primary

Measure	Time frame
1. Patient background 2. Roentgenographic cephalogram 3. Adverse event	—

Secondary

Measure	Time frame
1. Research subjects questionnaire (DAS59, ADL, SDS) 2. Evaluation of autologous tissue (cartilage or bone) harvest site 3. Palpation 4. Standard facial photograph 5. head computerized tomography (CT) 6. head magnetic resonance imaging (MRI)	—

Countries

Japan

Contacts

Public ContactReiko Hirabayashi

FUJI SOFT INCORPORATED

reikohir@fsi.co.jp+81-50-3000-2750

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026