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Immediate placement of a single-tooth implant after extraction in the aesthetic zone

Immediate placement and/or restoration of a single-tooth implant after extraction in the anterior maxilla: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN57251089
Enrollment
76
Registered
2012-02-09
Start date
2010-10-06
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Failing tooth in the aesthetic zone Oral Health Disorders of tooth development and eruption

Interventions

2 groups with suffcient bone and 2 groups with insufficient bone. They are randomised depending on the bony defect. An envelope is opened after the bony defect is determined. 1. Sufficient bone: the

Sponsors

University Medical Centre Groningen (Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient is 18 years or older 2. The replacing tooth is an incisor (central or lateral), a canine or a first premolar in the maxilla. The adjacent teeth are natural teeth 3. The implant site must be free from infection 4. Adequate oral hygiene 5. Sufficient mesio-distal, bucco-lingual, and interocclusal space for placement of an anatomic restoration 6. The patient is capable of understanding and giving informed consent

Exclusion criteria

Exclusion criteria: 1. Medical and general contraindications for the surgical procedures 2. Presence of an active and uncontrolled periodontal disease 3. Presence of pathologic microflora 4. Bruxism 5. Site of implant placement is an extraction wound younger than three months 6. Smoking (patients who stop smoking six weeks before the operation can be included) 7. A history of local radiotherapy to the head and neck region

Design outcomes

Primary

MeasureTime frame
Changes in peri-implant hard tissues (marginal bone levels, mesial and distal)

Secondary

MeasureTime frame
1. Implant survival 2. Peri-implant soft tissues (modified Plaque-index, modified Bleeding-Index, papil index, probing depth,recession, width of keratinized epithelium) 3. Patient satisfaction (OHIP-14) 4. Aesthetic Index (Meijer et al. 2005)

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 4, 2026