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Associations of Alveolar Bone Loss and Interleukin-1β Levels in One and Two Stage Surgical Procedures

Primary Purpose

Implant Infection, Alveolar Bone Loss

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
tissue level dental implant
Bone level dental implant
Sponsored by
Firat University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Implant Infection focused on measuring one stage dental implant, two stage dental implant, Interleukin-1β

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • patients in the study who had one tooth absent in the mandible
  • patients in the study should be least 18 years old.

Exclusion Criteria:

Patients in the study were the absence of the following points;

  • poor mouth hygiene,
  • bruxism, dental implants,
  • chemotherapy or radiotherapy,
  • addictions (alcohol, cigarettes, and medications),
  • disease in the jawbones observed clinically or radiographically,
  • pregnancy,
  • antibiotic and/or anti-inflammatory medication use in the last three months.

Sites / Locations

  • Dicle University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Tissue level dental implant

Bone level dental implant

Arm Description

Tissue level dental implants (Straumann AG, Waldenburg, Switzerland) were inserted in patients group I (n=20).

Bone level dental implants (Straumann AG, Waldenburg, Switzerland ) were inserted in patients group II (n=20).

Outcomes

Primary Outcome Measures

change of alveolar bone level
The primary outcome of the study was a change in alveolar bone level (height in mm) at the 40 implant site between T0 and T2 months after surgery measured on CBCT. All measurements were performed at four sites (mesial, distal, buccal, and lingual) around each dental implant at T0 and T2. These four values were then averaged for each dental implant. Alveolar bone level were measured in millimeters (height in mm) from a fixed reference point on the implant (implant shoulder to the most coronal position of the crestal bone contacting the implant).

Secondary Outcome Measures

changes level of IL-1β
The secondary outcome of the study was change the level of IL-1β pg/ml between T0, T1, and T2. To obtain PICF, filter paper strips were gently inserted into the peri-implant crevice for 30 s at the mesial, distal, buccal, and lingual sites of the dental implant. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. The level of IL-1β pg/ml (weight in picogram, weight in milliliter)
changes of PPD
The secondary outcome of the study was change of the PPD between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Probing pocket depth (PPD) (depth in mm), were measured
changes of Modified plaque index
The secondary outcome of the study was change of the Modified plaque index between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Modified plaque index (0=no plaque, 1= mild plaque, 2= moderate plaque, 3=severe plaque).
changes of Modified gingival index
The secondary outcome of the study was change of the Modified gingival index between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Modified gingival index (0=healthy, 1=mild inflammation 2= moderate inflammation 3=severe inflammation).
changes of Modified bleeding index
The secondary outcome of the study was change of the Modified bleeding index between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Modified bleeding index (0= no bleeding, 1= mild bleeding, 2= moderate bleeding, 3=severe bleeding).

Full Information

First Posted
January 25, 2017
Last Updated
February 6, 2017
Sponsor
Firat University
Collaborators
Dicle University
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1. Study Identification

Unique Protocol Identification Number
NCT03045458
Brief Title
Associations of Alveolar Bone Loss and Interleukin-1β Levels in One and Two Stage Surgical Procedures
Official Title
Associations of Alveolar Bone Loss, Clinical Parameters and Interleukin-1β Levels in One and Two Stage Surgical Procedures: A Randomized Prospective Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
September 1, 2010 (Actual)
Primary Completion Date
October 1, 2010 (Actual)
Study Completion Date
June 1, 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Firat University
Collaborators
Dicle University

4. Oversight

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

5. Study Description

Brief Summary
The present study was compared the level of alveolar bone loss, clinical parameters and IL-1β in PICF in one- or two-stage surgical procedures. Half of the patients were performed tissue level implant while other half were performed bone level implant.
Detailed Description
The present study included 40 healthy patients (24 males and 16 females; mean age, 30.75 ± 8.58 years) who had one tooth absent in the mandible, at the Department of Periodontology, Dicle University, Diyarbakir, Turkey, between 2010 and 2011. All patients were informed in detail about the study protocol, and they were asked to sign informed consent forms. Ethics committee approval was obtained from Dicle University Ethics Committee for this study (D.Ü.D.F.E.K.2010/02) This study was designed as a prospective, randomized, controlled study. Randomization was performed prior to surgery by opening a sequentially numbered sealed envelope corresponding to the patient recruitment number. Investigators received randomization instructions only after enrolling a subject and immediately prior to surgery. The participants were randomly divided into two groups. A one-stage surgical procedure was performed on 20 patients (Group I) and a two-stage surgical procedure was performed on the other 20 patients (Group II). The primary outcome of the study was a change in alveolar bone level at the implant site between T0 and T2 months after surgery measured on CBCT. The secondary outcomes between T0, T1, and T2 were changes the level of IL-1β PICF, probing pocket depth (PPD), modified plaque index (mPI), modified gingival index (mGI), and modified bleeding index (mBI). All implants (Straumann AG, Waldenburg, Switzerland) were inserted by the same periodontist (T.T.Y.) in the present study. Pre-surgical radiographic evaluation was conducted using CBCT. Before surgery, the patient's mouth was rinsed with chlorhexidine mouthwash. After local anesthesia, full thickness flaps were reflected, and osteotomies were prepared in the first mandibular molar sites. In these surgical operations, 20 tissue-level and 20 bone-level dental implants 12 mm in length and 4.8 mm in diameter were inserted in Group I and Group II, respectively. Three months later, second-stage surgery was performed and implant exposed into the oral cavity. Cover screw was removed and replaced with healing abutments. Three months waited for second surgery in bone level implants. Patients of both groups were enrolled in a monthly periodontal/peri-implant maintenance program after abutments were connected in which, full mouth scaling was performed around all natural teeth and implant surfaces. Oral hygiene instructions regarding regular tooth brushing were given and patients were encouraged to floss the teeth and periimplant surfaces daily. There was no implant failed during the study and adverse event of these treatments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Implant Infection, Alveolar Bone Loss
Keywords
one stage dental implant, two stage dental implant, Interleukin-1β

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
In the surgical operations, 20 tissue-level and 20 bone-level dental implants 12 mm in length and 4.8 mm in diameter were inserted in Group I and Group II, respectively.
Masking
None (Open Label)
Masking Description
Only the surgeon knows detail about the groups of participants. Participant, care provider,outcomes assessor have no knowledge of groups
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tissue level dental implant
Arm Type
Active Comparator
Arm Description
Tissue level dental implants (Straumann AG, Waldenburg, Switzerland) were inserted in patients group I (n=20).
Arm Title
Bone level dental implant
Arm Type
Active Comparator
Arm Description
Bone level dental implants (Straumann AG, Waldenburg, Switzerland ) were inserted in patients group II (n=20).
Intervention Type
Device
Intervention Name(s)
tissue level dental implant
Other Intervention Name(s)
Straumann AG, Waldenburg, Switzerland, dental implant
Intervention Description
After local anesthesia, full thickness flaps were reflected, and osteotomies were prepared in the first mandibular molar sites. In these surgical operations, 20 tissue-level implants 12 mm in length and 4.8 mm in diameter were inserted in Group I. Cover screw was removed and replaced with healing abutments.
Intervention Type
Device
Intervention Name(s)
Bone level dental implant
Other Intervention Name(s)
Straumann AG, Waldenburg, Switzerland, dental implant
Intervention Description
After local anesthesia, full thickness flaps were reflected, and osteotomies were prepared in the first mandibular molar sites. In these surgical operations, 20 bone-level dental implants 12 mm in length and 4.8 mm in diameter were inserted inGroup II. Three months later, second-stage surgery was performed and implant exposed into the oral cavity. Cover screw was removed and replaced with healing abutments. Three months waited for second surgery in bone level implants.
Primary Outcome Measure Information:
Title
change of alveolar bone level
Description
The primary outcome of the study was a change in alveolar bone level (height in mm) at the 40 implant site between T0 and T2 months after surgery measured on CBCT. All measurements were performed at four sites (mesial, distal, buccal, and lingual) around each dental implant at T0 and T2. These four values were then averaged for each dental implant. Alveolar bone level were measured in millimeters (height in mm) from a fixed reference point on the implant (implant shoulder to the most coronal position of the crestal bone contacting the implant).
Time Frame
0 and 6 month
Secondary Outcome Measure Information:
Title
changes level of IL-1β
Description
The secondary outcome of the study was change the level of IL-1β pg/ml between T0, T1, and T2. To obtain PICF, filter paper strips were gently inserted into the peri-implant crevice for 30 s at the mesial, distal, buccal, and lingual sites of the dental implant. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. The level of IL-1β pg/ml (weight in picogram, weight in milliliter)
Time Frame
0, 3, and 6 month
Title
changes of PPD
Description
The secondary outcome of the study was change of the PPD between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Probing pocket depth (PPD) (depth in mm), were measured
Time Frame
0, 3, and 6 month
Title
changes of Modified plaque index
Description
The secondary outcome of the study was change of the Modified plaque index between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Modified plaque index (0=no plaque, 1= mild plaque, 2= moderate plaque, 3=severe plaque).
Time Frame
0, 3, and 6 month
Title
changes of Modified gingival index
Description
The secondary outcome of the study was change of the Modified gingival index between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Modified gingival index (0=healthy, 1=mild inflammation 2= moderate inflammation 3=severe inflammation).
Time Frame
0, 3, and 6 month
Title
changes of Modified bleeding index
Description
The secondary outcome of the study was change of the Modified bleeding index between T0, T1, and T2. A Williams periodontal probe was used for all clinical measurements.These parameters were recorded for evaluating the clinical status of the dental implants. All measurements were performed at four sites around each dental implant. For the statistical analysis, median of the four measurements at each implant was used. Modified bleeding index (0= no bleeding, 1= mild bleeding, 2= moderate bleeding, 3=severe bleeding).
Time Frame
0, 3, and 6 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: patients in the study who had one tooth absent in the mandible patients in the study should be least 18 years old. Exclusion Criteria: Patients in the study were the absence of the following points; poor mouth hygiene, bruxism, dental implants, chemotherapy or radiotherapy, addictions (alcohol, cigarettes, and medications), disease in the jawbones observed clinically or radiographically, pregnancy, antibiotic and/or anti-inflammatory medication use in the last three months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
tuba talo yıldırım
Organizational Affiliation
Dicle University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dicle University
City
Diyarbakir
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data can not be used another purpose such as meta-analyses, reanalysis, or replication of results.
Citations:
PubMed Identifier
28826290
Citation
Talo Yildirim T, Acun Kaya F, Yokus B, Colak M, Ozdemir Kaya E, Tekin G, Saribas E, Uysal E, Guncu GN. Associations of alveolar bone loss and interleukin-1beta levels in one- and two-stage surgical procedures: a randomized prospective trial. Acta Odontol Scand. 2017 Nov;75(8):608-615. doi: 10.1080/00016357.2017.1367959. Epub 2017 Aug 21.
Results Reference
derived
Available IPD and Supporting Information:
Available IPD/Information Type
Clinical Study Report
Available IPD/Information URL
http://mc.manuscriptcentral.com/jperio

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Associations of Alveolar Bone Loss and Interleukin-1β Levels in One and Two Stage Surgical Procedures

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