Evaluation of new iranian implant system

Clinical and radiografic evaluation of new iranian implant system (sina bionic) in partially edentolous patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20151017024573N5

Enrollment

Registered

2018-08-17

Start date

2018-09-23

Completion date

Unknown

Last updated

2018-09-11

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

Conditions

Edentolous. Loss of teeth due to accident, extraction or local periodontal disease

Interventions

Intervention group: new Iranian implant(SINA BIONIC) insertion made by Niktash Asia.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Short 3 unit bridge or single edentolous 1 mm bone around implant

Exclusion criteria

Exclusion criteria: Augmentation in implant site Infection in implant site Smokers uncontrolled dibetic patients or any disorders that affect treatment results Bisphosphonate intake Active periodontal disease bruxism or clenching Pregnancy

Design outcomes

Primary

Measure	Time frame
Bleeding on probing. Timepoint: 6 and 12 month after implant insertion. Method of measurement: probe.;Bone level at mesial and distal of implant. Timepoint: immediately after surgery and 6 and 12 month later. Method of measurement: periapical radiography.;Pocket depth. Timepoint: 6 and 12 month after implant placement. Method of measurement: probe.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohadeseh Heidari

Tehran University of Medical Sciences

heidari_mohadeseh@yahoo.com+98 21 8897 8351

Outcome results

None listed

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