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Histological and radiographic studies on the effect of new bone repair materials for guiding bone regeneration (GBR)

Histological and radiographic studies on the effect of new bone repair materials for guiding bone regeneration (GBR)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013061
Enrollment
Unknown
Registered
2017-10-20
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

alveolar bone defect

Interventions

test group:Heal-All bone repair material
Control group:Bio-Oss

Sponsors

Hospital of Stomatology of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1) with both sides of the jaw are required to remove the posterior teeth (molar or premolars), and the need for line repair patients; 2) Alveolar fossa at least three walls, and any side of the bone wall defects do not exceed two-thirds; 3) after tooth extraction with periodontal probe to measure the depth of alveolar fossa = 6 mm; 4) patients with good oral environment, good compliance; 5) Aged 18-55 years male and female; 6) Patients who voluntarily participate in and sign "informed consent" after obtaining full knowledge.

Exclusion criteria

Exclusion criteria: 1) have serious heart, liver, lung, kidney and other vital organs or severe blood, immune, endocrine (such as: uncontrollable diabetes) and other systemic diseases; 2) A history of chronic disease treatment known to affect oral environmental drugs (eg phenytoin, dihydropyridine calcium antagonists, cyclosporine, nonsteroidal anti-inflammatory drugs) within 1 month prior to enrollment (= 2 weeks); 3) suffering from bone metabolic diseases (such as: osteoporosis, deformed osteitis, etc.), or within 1 month before taking the drug can significantly affect the bone metabolism of drugs or products (such as steroids, bisphosphonates); 4) 6 months before enrollment with severe smoking history (> 10 / day); 5) alcohol or long-term drug abusers; 6) pregnant or lactating women; 7) allergic constitution, with collagen allergy or other serious allergic reactions past history; 8) have mental illness or mental disorders; 9) severe periodontal disease, and can not be effective control; 10) oral inflammation, infection can not control; 11) history of head and neck radiotherapy; 12) Other patients who have been judged by the investigator who are not eligible for inclusion.

Design outcomes

Primary

MeasureTime frame
Micro-CT observation and analysis of indicators;Histological observation and analysis of indicators;CBCT observation of bone mass analysis of indicators;

Secondary

MeasureTime frame
Implant stability analysis index;Clinical observation;

Countries

China

Contacts

Public ContactBin Shi
shibin_dentist@whu.edu.cn+86 13808643395

Outcome results

None listed

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