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A Non-Inferiority Study on Collagen Matrix (Mucograft) Versus Autogenous Connective Tissue Graft for Soft-Tissue Management in Alveolar Ridge Preservation in the Anterior Esthetic Zone

A Clinical Controlled Study on the Effectiveness of Collagen Matrix (Mucograft) as a Substitute for Autogenous Connective Tissue Graft in Soft-Tissue Management During Alveolar Ridge Preservation in the Anterior Esthetic Zone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113768
Enrollment
Unknown
Registered
2025-12-03
Start date
2025-12-09
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

defect of dentition

Interventions

Control group:The control group will receive soft?tissue augmentation after tooth extraction using an autogenous palatal soft?tissue graft
Test group:Soft?tissue augmentation after tooth extraction will be performed using the Mucograft collagen matrix

Sponsors

Beijing Stomatological Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients requiring extraction of a single maxillary anterior tooth due to caries, endodontic complications, or trauma, who elect implant-supported restoration, with natural teeth present on both adjacent sides. 2.Age 18–65 years, both sexes eligible. 3:.Good oral hygiene, with a Plaque Index < 2 and bleeding on probing sites < 20%.

Exclusion criteria

Exclusion criteria: 1. Immediate probing/CBCT assessment prior to or following extraction confirms integrity of labial, palatal (lingual) and adjacent bone plates, with a minimum 2mm labial bone plate thickness. Candidates meeting clinical and radiographic criteria for immediate implant placement. 2. Presence of active or uncontrolled periodontal disease (PD >=4 mm), or acute infection at the target site; 3. Smoking habit (>10 cigarettes/day); 4. Surgical contraindications, history of head and neck radiotherapy, uncontrolled systemic diseases (e.g., diabetes mellitus), systemic conditions or medications affecting soft/hard tissue healing (e.g., bisphosphonate use); 5. Pregnant or lactating women; 6. Individuals with mental or intellectual disabilities; 7. History of allergic reactions to porcine or other animal-derived collagen/gelatin/blood products; 8. Religious prohibitions (e.g., Islam, Judaism) against porcine-derived materials.

Design outcomes

Primary

MeasureTime frame
Changes in alveolar bone dimensions and external soft?tissue contour;

Secondary

MeasureTime frame
Esthetic outcomes;

Countries

China

Contacts

Public ContactZhenhua Gao

Beijing Stomatological Hospital, Capital Medical University

gaozhenhua2211@126.com+86 187 2839 3829

Outcome results

None listed

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