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Bone Healing at Non-submerged Implants Installed With Different Insertion Torques.

Primary Purpose

Edentulous; Alveolar Process, Atrophy

Status
Completed
Phase
Not Applicable
Locations
Colombia
Study Type
Interventional
Intervention
implant installation
Sponsored by
ARDEC Academy
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Edentulous; Alveolar Process, Atrophy

Eligibility Criteria

25 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • presence of at least two edentulous zone in the posterior segment of the mandible
  • ≥ 25 years of age
  • smoking ≤ 10 cigarettes per day
  • Good general health
  • No contraindication for oral surgical procedures.
  • Not being pregnant.

Exclusion Criteria:

  • Presence of systemic disorders
  • Chemotherapy or radiotherapy;
  • Smokers >10 cigarettes per day
  • Previous bone augmentation procedures in the region

Sites / Locations

  • Colombia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Test site (torque of <10 Ncm)

Control site (torque of ~30 Ncm)

Arm Description

The test sites (<10 Ncm) will be over-prepared with drills of larger diameter

the standard sites (~30 Ncm)will be prepared with the corresponding drills suggested by the manufacturer

Outcomes

Primary Outcome Measures

New bone in contact with the implant surface
The percentages of new bone will be evaluated both in contact with the implant surface

Secondary Outcome Measures

Bone density around the implant surface
The total mineralized bone will be assessed as sum of new and old bone

Full Information

First Posted
July 10, 2019
Last Updated
July 11, 2019
Sponsor
ARDEC Academy
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1. Study Identification

Unique Protocol Identification Number
NCT04017156
Brief Title
Bone Healing at Non-submerged Implants Installed With Different Insertion Torques.
Official Title
Bone Healing at Non-submerged Implants Installed With Different Insertion Torques. A Split Mouth Histomorphometric Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
July 20, 2016 (Actual)
Primary Completion Date
November 22, 2016 (Actual)
Study Completion Date
October 17, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ARDEC Academy

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of the study is to evaluate histomorphometrically the healing at implants installed with standard or very low insertion torque values.
Detailed Description
Very high insertion torque values have been recommended when immediate loading is applied to implants.1 However, it has been shown that similar clinical outcomes may be achieved even with insertion torque values ≤15 Ncm when implants are splinted together. Due to the contradictory outcomes on the influence of the torque on osseointegration and a lack of histological data in humans, there is a need of more evidences that may support the clinicians in the decision making when an unintentional low insertion torque occur at implants during the daily practice. So the aim of the study i evaluate histomorphometrically the healing at implants installed in Twelve volunteer patients that will be recruited. Two screw-shaped titanium devices will be installed in the distal segments of the mandible using insertion torque values of either <10 Ncm or ~30 Ncm. The implants were left to heal in a non-submerged fashion. After 8 weeks, biopsies will be retrieved and ground sections will be prepared for histological evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Edentulous; Alveolar Process, Atrophy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Clinical Trial
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The two recipient sites will be selected prior the surgery, while the type of site preparation will be randomly decided. The randomization will be performed electronically (randomization.com) by a researcher neither involved in the selection of the patients nor in installation of the devices (DB). Sealed opaque envelopes will be prepared and opened at the time of surgery by an author not involved in the surgery (DB). Surgeon and patients will be blinded.
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Test site (torque of <10 Ncm)
Arm Type
Experimental
Arm Description
The test sites (<10 Ncm) will be over-prepared with drills of larger diameter
Arm Title
Control site (torque of ~30 Ncm)
Arm Type
Other
Arm Description
the standard sites (~30 Ncm)will be prepared with the corresponding drills suggested by the manufacturer
Intervention Type
Procedure
Intervention Name(s)
implant installation
Other Intervention Name(s)
implant surgery
Intervention Description
All site preparations will be performed deeper compared to the length of the implant so that the implant apex cannot reach the bottom of the osteotomy.
Primary Outcome Measure Information:
Title
New bone in contact with the implant surface
Description
The percentages of new bone will be evaluated both in contact with the implant surface
Time Frame
After 8 weeks of healing
Secondary Outcome Measure Information:
Title
Bone density around the implant surface
Description
The total mineralized bone will be assessed as sum of new and old bone
Time Frame
After 8 weeks of healing
Other Pre-specified Outcome Measures:
Title
pre-existing (old) bone, soft tissue (marrow spaces, Haversian canals, BMUs canals), bone debris/ clot remnants, and marrow spaces (soft tissue)
Description
The percentages of pre-existing (old) bone, soft tissue (marrow spaces, Haversian canals, BMUs canals), bone debris/ clot remnants, and marrow spaces (soft tissue) will be evaluated all in contact with the implant surface
Time Frame
After 8 weeks of healing

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: presence of at least two edentulous zone in the posterior segment of the mandible ≥ 25 years of age smoking ≤ 10 cigarettes per day Good general health No contraindication for oral surgical procedures. Not being pregnant. Exclusion Criteria: Presence of systemic disorders Chemotherapy or radiotherapy; Smokers >10 cigarettes per day Previous bone augmentation procedures in the region
Facility Information:
Facility Name
Colombia
City
Cartagena de Indias
State/Province
Cartagena
ZIP/Postal Code
5710
Country
Colombia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Will be shared after publication
Citations:
PubMed Identifier
21841994
Citation
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derived

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Bone Healing at Non-submerged Implants Installed With Different Insertion Torques.

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