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Alveolar Ridge Preservation without Barrier Membrane: A Randomised Controlled Clinical Trial

Alveolar Ridge Preservation without Barrier Membrane: A Randomised Controlled Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013528
Enrollment
Unknown
Registered
2017-11-24
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-11-27

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

Conditions

Partial edentulism

Interventions

Control:Alveolar ridge preservation with Bio-Oss Collagen and barrier membrane
Intervention:Alveolar ridge preservation with Bio-Oss Collagen

Sponsors

Department of Prosthodontics, Hospital of Stomatology, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Aged 20 to 70 year-old male or female; (2) Insufficient bone volume for immediate or early implant placement; (3) At least one tooth requires extraction, with indication of alveolar ridge preservation; (4) Extracted tooth can be incisors, canines, premolars or molars in upper or lower jaw (3rd molar excluded); (5) Reasons for extraction could be caries, tooth defect, endodontic complications, periapical disease or chronic periodontitis, and 3 bone wall should be intact for extracted site; (6) Adequate oral hygiene (Bleeding on probing = 20%; Plaque index = 20%); (7) Willingness to attend the trial.

Exclusion criteria

Exclusion criteria: (1) Unwillingness to be enrolled; (2) Tobacco usage over 10/d; (3) Extracted tooth is 3rd molar, deciduous tooth, supernumerary tooth, impacted tooth, malposed tooth, orthodontically extracted tooth, disused tooth, or other tooth without need for restorations; (4) Extraction sites with no plan for implant restorations are deemed unnecessary for ARP; (5) Extraction sites with ideal bone envelope for immediate implant placement are deemed unnecessary for ARP; (6) Extraction sites with sufficient bone for early or conventional implant placement are deemed unnecessary for ARP; (7) Allergy to bone graft or collagen membrane; (8) Medical history that contraindicated oral surgical treatment (for example, severe heart disease, malignant tumor, hemorrhagic disease, coagulation disturbance, acute infectious disease, etc), or pregnancy for female participants; (9) Patients enrolled in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Alveolar bone resorption in different horizontal and vertical levels;

Secondary

MeasureTime frame
Keratinized gingiva reduction;Marginal bone reduction;Incidence of adverse events;

Contacts

Public ContactZhao Ke

Hospital of Stomatology, Sun Yat-sen University

zhaoke@mail.sysu.eud.cn+86 13928860925

Outcome results

None listed

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