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CGF and a/iPRF in oral implant bone grafting surgery

CGF and a/iPRF in oral implant bone grafting surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070107
Enrollment
Unknown
Registered
2023-04-03
Start date
2020-12-03
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Bone Defects

Interventions

control group:No
Deproteinized bovine bone mineral group (DBBM group) :Add deproteinized bovine bone mineral (DBBM) only.
CGF group( concentrated growth factors group) :Add concentrated growth factor(CGF)
liquid concentrated growth factor together with deproteinized bovine bone mineral group(LPCGF+DBBM group):Add liquid concentrated growth factor (LPCGF) together with deproteinized bovine bone mineral
Concentrated growth factor together with deproteinized bovine bone mineral group(CGF+DBBM group):Add concentrated growth factor(CGF) together with deproteinized bovine bone mineral (DBBM).
liquid concentrated growth factor together with deproteinized bovine bone mineral together with CGF group(LPCGF+DBBM+CGF group):Add liquid concentrated growth factor (LPCGF) together with deproteiniz

Sponsors

Chongqing Medical University Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 76 Years

Inclusion criteria

Inclusion criteria: Age >= 18 years; maxillary molars or premolars missing and well healed; no cysts or inflammation in the maxillary sinus on preoperative CBCT; reduced RBH and inability to place >8.5mm implants; no smoking, alcohol or other bad habits; no history of radiotherapy in the head and neck, normal preoperative blood count and glucose; no moderate, severe or uncontrolled periodontal disease with good plaque control; no systemic diseases that are not suitable for oral surgery systemic diseases.

Exclusion criteria

Exclusion criteria: Does not meet the inclusion criteria (1) Unable to understand the experimental content or withdrew in the middle of the experiment (2) Intolerant of systemic diseases (3) Those who have a history of radiation therapy and are receiving radiation therapy and immunosuppressive therapy (4) Severe periodontitis or poor oral hygiene (5) Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Cone beam computed tomography;

Secondary

MeasureTime frame
Planting success rate;Aesthetic evaluation criteria;

Countries

China

Contacts

Public ContactXu Binting
bintingxu@hospital.cqmu.edu.cn18523868227

Outcome results

None listed

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