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Efficacy of pure xenografts in bone augmentation

Efficacy of xenograft materials in maxillary edentulous ridge augmentation: a clinical study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211122053149N2
Enrollment
15
Registered
2023-09-18
Start date
2023-09-06
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Horizontal defect in maxillary ridge.

Interventions

Local anesthesia is administered in the maxilla by injection of 4% articaine plus 1:100,000 epinephrine. A mid-crestal incision is made from the most anterior tooth to 5 mm beyond the augmentation are

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Partial/complete edentulism of the maxillary ridge with or without the need for maxillary sinus floor augmentation Patients requiring implant-supported fixed dentures Availability of follow-up data of patients for a minimum of 6 months after edentulous ridge augmentation.

Exclusion criteria

Exclusion criteria: Smoking Alcohol consumption Substance abuse Uncontrolled metabolic disorders Untreated periodontal disease History of radiotherapy or intake of immunosuppressants History of intake of anti-resorptive medications

Design outcomes

Primary

MeasureTime frame
Buccolingual width of the ridge at the level of 2 mm apical to the alveolar crest. Timepoint: Measurement of ridge width at the beginning of treatment and at least 6 months after surgery. Method of measurement: Cone beam computed tomography.

Secondary

MeasureTime frame
Ridge height based on a fixed point on the nasal floor or sinus floor. Timepoint: At the beginning of treatment and at least 6 months after surgery. Method of measurement: Cone beam computed tomography.;Height increase in the sinus area in cases where sinus augmentation would also been performed. Timepoint: At the beginning of treatment and at least 6 months after surgery. Method of measurement: Cone beam computed tomography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAnahita Moscowchi

Shahid Beheshti University of Medical Sciences

a.moscowchi@gmail.com+98 21 2990 2314

Outcome results

None listed

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