About this trial
This study aims to characterise the stability of crestal bone levels one year after loading, the associated aesthetic outcomes, immunological response, prosthodontic outcomes as well as overall patient reported outcome measures for modSLA (SLActive, Institut Straumann AG, Switzerland) and NGA (TiUltraNP, Nobel Biocare AG, Switzerland) dental implants.
Eligibility criteria
Qualifiers
Age: over 18 years old,
Gender: male and female.
Patient must be able and willing to follow study procedures and instructions and have capacity to provide informed consent.
Patient must require tooth extraction of a maxillary first premolar or single-rooted anterior tooth as the result of caries, endodontic failure or trauma
Disqualifiers
Systemic disease that can interfere with dental implant therapy (e.g. uncontrolled diabetes)
2 adjacent teeth requiring extraction
Greater than one wall of the socket missing - assessed at time of extraction
Any contraindications for oral surgical procedures
Trial design
Treatments tested in this trial
- Implant Type
Treatment groups
Sponsors and collaborators
Barts & The London NHS Trust
Lead sponsor
Virginia Commonwealth University
Collaborator