Evaluation of the effect of polyethylene prosthesis on volume changes in mid-facial area

Evaluation of the effect of polyethylene prosthesis surgery on volume changes in mid-facial area in bouali hospital patients by 3D scanner

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180515039664N1

Enrollment

Registered

2018-05-28

Start date

2018-06-05

Completion date

Unknown

Last updated

2018-06-18

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

Conditions

Midface Deficiency. Congenital malformation of face and neck, unspecified

Interventions

Intervention group: Surgical placement of polyethylene prosthesis Design M Malar Implants(MEDPOR MEDPOR™, Porex Surgical Inc, Newnan USA) Small 9507 ? 9508 (64mm19mm3mm) and 3D scan of face surface.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients requiring surgical prosthetics referring to Boouli Hospital No systemic disease limiting ASA1 or ASA2 classifications No history of surgery or trauma in the head and neck area

Exclusion criteria

Exclusion criteria: Infection or displacement of the prosthesis after surgery BMI changes over one unit in the follow-up period

Design outcomes

Primary

Measure	Time frame
Volume of the midfacial area. Timepoint: Measuring the volume of the face will be done before surgery and 5 months after surgery. Method of measurement: 3D scanner device Structured Light (Sense™, 3D Systems Inc, Rock Hill, USA).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSina Hakimi

Islamic Azad University

sinahakimi@irimc.org+98 21 3331 1107

Outcome results

None listed

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