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the outcome of fronto-orbital advancement in patients with non-syndromic anterior plagiocephaly

Evaluation of esthetic and anthropometric outcomes of frontorbital correction for non-syndromic anterior plagiocephaly by modified z technique of temporal region osteotomy in 15khordad and Mofid hospitals during 2022-2024

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110522006552N3
Enrollment
49
Registered
2024-01-23
Start date
2024-01-21
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Patients with Non- syndromic anterior plagiocephaly. Congenital malformations and deformations of the musculoskeletal system

Interventions

Intervention group: For all patients with non-syndromic plagiocephaly, a coronal incision is first given so that the frontal bone can be moved after the flap is raised and turned down to 5 cm above th

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Months to 24 Months

Inclusion criteria

Inclusion criteria: Written informed consent to undergo the surgical procedure Patients with anterior plagiocephaly were referred to the clinic in 15 Khordad and Mofid hospitals in Tehran between 2021 and 2023. According to the opinion of the plastic surgeon, patients with craniosynostosis who are candidates for correction with front orbital advancement.

Exclusion criteria

Exclusion criteria: Multi- suture craniosynostosis Syndromic craniosynostosis

Design outcomes

Primary

MeasureTime frame
Surgical and aesthetic satisfaction score. Timepoint: Before surgery and 3 months after intervention (surgery). Method of measurement: Satisfaction level questionnaire.;Anthropometric skull measurements. Timepoint: Before surgery and 6 months after intervention (surgery). Method of measurement: Using a graduated ruler.

Secondary

MeasureTime frame
Recurrence of deformity after surgery. Timepoint: 12 month after intervention. Method of measurement: Physical Examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehran Noori

Shahid Beheshti University of Medical Sciences

mehrannoori64@yahoo.com+98 21 2243 9982

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026