Recruitment

Recruitment Status
Completed

Inclusion Criterias

Have one non-molar tooth requiring extraction that will be replaced by a dental implant. The site must be bordered by at least one tooth.
Healthy male or female who is at least 18 years old.
Have one non-molar tooth requiring extraction that will be replaced by a dental implant. The site must be bordered by at least one tooth.
Healthy male or female who is at least 18 years old.

Exclusion Criterias

Patients with debilitating systemic diseases, or diseases that have a clinically significant effect on the periodontium.
Previous head and neck radiation therapy.
Patients who are currently taking IV bisphosphonates or who had IV treatment with bisphosphonates irrespective of duration.
...
Patients with debilitating systemic diseases, or diseases that have a clinically significant effect on the periodontium.
Previous head and neck radiation therapy.
Patients who are currently taking IV bisphosphonates or who had IV treatment with bisphosphonates irrespective of duration.
Patients on long term NSAID (nonsteroidal anti-inflammatory drug) or steroid therapy.
Patients who have been treated with oral bisphosphonates for more than three years.
Patients with an allergy to any material or medication used in the study.
Patients who need prophylactic antibiotics.
Presence or history of osteonecrosis of jaws.
Chemotherapy in the previous 12 months.
Pregnant patients. -

Summary

Conditions
Clinical Efficacy
Type
Interventional
Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Masking: Single (Outcomes Assessor)
  • Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Patient Selection 30 patients will be selected that meet the following criteria: Inclusion Criteria Have one non-molar tooth requiring extraction that will be replaced by a dental implant. The site must be bordered by at least one tooth. Healthy male or female who is at least 18 years old. Patients ...

Patient Selection 30 patients will be selected that meet the following criteria: Inclusion Criteria Have one non-molar tooth requiring extraction that will be replaced by a dental implant. The site must be bordered by at least one tooth. Healthy male or female who is at least 18 years old. Patients must sign an informed consent approved by the University of Louisville Human Studies Committee. Exclusion Criteria Patients with debilitating systemic diseases, or diseases that have a clinically significant effect on the periodontium. Presence or history of osteonecrosis of jaws. Patients who are currently taking IV bisphosphonates or who had IV treatment with bisphosphonates irrespective of duration. Patients who have been treated with oral bisphosphonates for more than three years. Patients with an allergy to any material or medication used in the study. Patients who need prophylactic antibiotics. Previous head and neck radiation therapy. Chemotherapy in the previous 12 months. Patients on long term NSAID or steroid therapy. Pregnant patients.

Inclusion Criterias

Have one non-molar tooth requiring extraction that will be replaced by a dental implant. The site must be bordered by at least one tooth.
Healthy male or female who is at least 18 years old.
Have one non-molar tooth requiring extraction that will be replaced by a dental implant. The site must be bordered by at least one tooth.
Healthy male or female who is at least 18 years old.

Exclusion Criterias

Patients with debilitating systemic diseases, or diseases that have a clinically significant effect on the periodontium.
Previous head and neck radiation therapy.
Patients who are currently taking IV bisphosphonates or who had IV treatment with bisphosphonates irrespective of duration.
...
Patients with debilitating systemic diseases, or diseases that have a clinically significant effect on the periodontium.
Previous head and neck radiation therapy.
Patients who are currently taking IV bisphosphonates or who had IV treatment with bisphosphonates irrespective of duration.
Patients on long term NSAID (nonsteroidal anti-inflammatory drug) or steroid therapy.
Patients who have been treated with oral bisphosphonates for more than three years.
Patients with an allergy to any material or medication used in the study.
Patients who need prophylactic antibiotics.
Presence or history of osteonecrosis of jaws.
Chemotherapy in the previous 12 months.
Pregnant patients. -

Locations

Louisvile, Kentucky, 40202
Louisvile, Kentucky, 40202

Tracking Information

NCT #
NCT01900964
Collaborators
Not Provided
Investigators
  • Principal Investigator: Henry Greenwell, DMD University of Louisville
  • Henry Greenwell, DMD University of Louisville