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Comparative histological and radiological results of two bone grafts used in maxillary sinus augmentation

Comparative histological and radiological results of Nano-crystalline hydroxyapatite (Ostim) and Bio-oss used in maxillary sinus augmentation: a human study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204157128N2
Enrollment
10
Registered
2012-12-10
Start date
2012-04-03
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

maxillary sinus augmentation due to bone resorbtion. Other osteopathies

Interventions

Intervention 1: control group: use of bio-oss in sinus augmentation. Intervention 2: Intervention:use of ostim in sinus augmentation.
Treatment - Surgery
control group: use of bio-oss in sinus augmentation
Intervention:use of ostim in sinus augmentation

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria; maxillary partial (unilateral or bilateral) edentulism or complete edentulism; Rresidual bone height between the sinus floor and the alveolar crest less than 5 mm. The exclusion criteria: smokers; pregnant women; maxillary sinus pathology; cystic lesions of the maxillary sinus; systemic disease; e.g unstable diabetes; heart disease; malignancies; radiotherapy for head and neck especially maxilla; autoimmune diseases; metabolic diseases that becomes difficult to the healing of the soft and hard tissue (e.g osteoporosis, hyperparathyroidism ,...); steroids and immunosuppressive drugs; bisphosphonates drug; untreated periodontal disease and periapical disease especially in teeth; which are close to the sinuses.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
New bone formation after sinus augmentation. Timepoint: After 5 month. Method of measurement: Microscope.

Secondary

MeasureTime frame
Residual bone graft after 5 month. Timepoint: After 5 month. Method of measurement: microscope.;Bone density. Timepoint: After 5 month. Method of measurement: CBCT.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Rahmanpour

Tabriz University of Medical Sciences

nasrin-rahmanpour@yahoo.comshirmohamadia@tbzmed.ac.ir+98 41 1335 5966

Outcome results

None listed

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