Increased Peri-implant Keratinized Mucosal Thickness at Different Operative Times
Primary Purpose
Dental Implants, Peri-Implantitis
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Subepithelial connective tissue graft
Sponsored by
About this trial
This is an interventional treatment trial for Dental Implants focused on measuring keratinized mucosa thickness, dental Implants, subepithelial connective tissue graft, marginal bone level
Eligibility Criteria
Inclusion Criteria:
- No systemic diseases or pregnancy;
- The thickness of keratinized mucosa where the posterior tooth is missing is less than 2 mm;
- Full-mouth plaque score (FMPS) < 20% (measured at four sites per tooth) and bleeding on probing score (BOP%) ≤25% (measured at six sites per tooth);
- Periodontal condition is stable, no probing depths ≥5 mm;
- No previous soft tissue augmentation procedure at experimental site;
- The patient has signed informed consent and accepts the operation of subepithelial connective tissue transplantation.
Exclusion Criteria:
- Patients with uncontrolled hypertension;
- Patients with uncontrolled diabetes;
- Patients with insufficient oral hygiene and Untreated periodontitis;
- Pregnant or lactating women;
- Smoker;
- Patients with long-term (> 6 months) use of glucocorticoids;
- History of malignancy, radiotherapy, or chemotherapy for malignancy within the past 5 years;
- Patients with severe cardiovascular problems;
- Patients with uncontrolled infectious or metabolic diseases;
- Patients with substance abuse.
Sites / Locations
- Department of Oral Medicine, the Second Affiliated Hospital, School of Medicine Zhejiang UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
treatment group 1
treatment group 2
Arm Description
At the same time of implant implantation, autologous tissue is transplanted into the recipient area by using Subepithelial connective tissue graft.
During the second stage operation, autologous tissue is transplanted into the recipient area by using Subepithelial connective tissue graft.
Outcomes
Primary Outcome Measures
peri-implant marginal bone level change
The bone level of the proximal and distal sites of the implant is measured by oral X-ray parallel projection method. Compare the image value with the actual value to calculate the actual bone level.
Secondary Outcome Measures
peri-implant clinical attachment level change
The distance between the reference point of impression edge and the bottom of gingival groove around the implant.
peri-implant keratinized mucosa width
keratinized tissue measured as the distance between muco-gingival junction and the gingival margin.
peri-implant keratinized mucosa thickness
gingival thickness measured 1.5 mm coronal to the MGJ using an injection needle, perpendicular to the tissue surface, with a silicon stop over the gingival surface.
peri-implant gingival index
Periodontal probe was used to measure 6 sites on buccal and lingual side each time to observe gingival color, texture and bleeding, and record the scores.
peri-implant gingival recession
The distance between the implant shoulder and the gingival margin of the temporary or final crown was measured with a periodontal probe (only when the implant shoulder was visible).
visual analogue scale
Visual analogous scale ( VAS) suggested by WHO was used to assess. Analgesia intensity expressed with 0-10, 0 point as without pain completely, 10 points as unbearable pain.
Full Information
NCT ID
NCT04683991
First Posted
December 22, 2020
Last Updated
December 15, 2021
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
1. Study Identification
Unique Protocol Identification Number
NCT04683991
Brief Title
Increased Peri-implant Keratinized Mucosal Thickness at Different Operative Times
Official Title
The Effect of Different Surgical Timing on the Clinical Efficacy of Increasing the Thickness of Keratinized Mucosa Around a Single Posterior Implant: a Prospective, Randomized Controlled Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 27, 2021 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Keratinized mucosa, which is composed of free gingiva and attached gingiva, is a barrier against bacterial invasion in oral cavity and provides good tissue sealing for periodontal environment. When the keratinized mucosa is insufficient, it is difficult to maintain the long-term stability of the implant, which is not conducive to the peri-implant health. It is generally believed that enough keratinized mucosa width is beneficial to reduce plaque accumulation and reduce the incidence rate of peri-implant diseases. In recent years, clinicians have gradually recognized that the thickness of keratinized mucosa plays an important role in maintaining the peri-implant health. Some researchers found that the thickness of mucosa is very important to maintain the aesthetic effect of implant restoration, and when the thickness of mucosa around the implant is less than 2mm, alveolar bone absorption will occur to maintain a stable biological width. A meta-analysis showed that when the thickness of the keratinized mucosa around the implant was greater than 2mm, the amount of marginal bone loss was significantly reduced (- 0.8mm, P < 0.0001).
It is considered that autogenous soft tissue graft is the most reliable technology to augment keratinized mucosa. Subepithelial connective tissue graft (SCTG) is a mucogingival surgery that transplant autologous free connective tissue under the pedicled semi thick flap to augment keratinized mucosa. It can effectively increase the thickness of soft tissue, cover the exposed implant, and reconstruct the interdental papilla. It is the gold standard for peri-implant soft tissue agumentation. Keratinized mucosal thickening surgery may be done prior to the surgical phase, after the surgical phase, before loading, or even after loading. It is believed that keratinized mucosal thickening at the same time of implantation can effectively reduce the possibility of mucosal recession after implantation, reduce the amount of marginal bone absorption in the process of osseointegration, which is conducive to maintaining the long-term stability of the implant. For the sake of clear clinical vision and convenient operation, clinicians often choose to thicken the keratinized mucosa during the secondary operation, and also obtain good postoperative effect. However, after the completion of the final repair, the keratinized mucosa thickening surgery increases the difficulty of operation and the technical requirements for the operator. In clinical practice, it is rarely selected to perform keratinized mucosal thickening at this time. At present, the effectiveness of timing on the outcome of soft tissue augmentation is still debated, and, most importantly, a direct comparison between simultaneous and staged procedures remains underexplored.
Therefore, this clinical trial is to prospectively compare the clinical efficacy of simultaneous versus delayed timing of soft tissue augmentation by SCTG placement around single implants, by evaluating the peri-implant marginal bone level change and soft tissue change, so as to provide reference for the formulation of clinical treatment plan and the selection of the best operation time.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Implants, Peri-Implantitis
Keywords
keratinized mucosa thickness, dental Implants, subepithelial connective tissue graft, marginal bone level
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
1:1 randomized controlled clinical trial were used. Random numbers generated by SPSS26.0 will be placed in sequentially coded, sealed, opaque envelopes. Only "1" or "0" will be generated, and the number of "1" or "0" generated by SPSS26.0 is 17. When the qualifications of the subjects were determined by the researchers, the envelopes were opened sequentially and the subjects were assigned to groups. The number "1" represented the treatment group 1 and the number "0" represented the treatment group 2.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
treatment group 1
Arm Type
Experimental
Arm Description
At the same time of implant implantation, autologous tissue is transplanted into the recipient area by using Subepithelial connective tissue graft.
Arm Title
treatment group 2
Arm Type
Experimental
Arm Description
During the second stage operation, autologous tissue is transplanted into the recipient area by using Subepithelial connective tissue graft.
Intervention Type
Procedure
Intervention Name(s)
Subepithelial connective tissue graft
Intervention Description
A de-epithelialized connective tissue graft is harvested from the homolateral palate and transplanted around the implant.
Primary Outcome Measure Information:
Title
peri-implant marginal bone level change
Description
The bone level of the proximal and distal sites of the implant is measured by oral X-ray parallel projection method. Compare the image value with the actual value to calculate the actual bone level.
Time Frame
18 months
Secondary Outcome Measure Information:
Title
peri-implant clinical attachment level change
Description
The distance between the reference point of impression edge and the bottom of gingival groove around the implant.
Time Frame
18 months
Title
peri-implant keratinized mucosa width
Description
keratinized tissue measured as the distance between muco-gingival junction and the gingival margin.
Time Frame
18 months
Title
peri-implant keratinized mucosa thickness
Description
gingival thickness measured 1.5 mm coronal to the MGJ using an injection needle, perpendicular to the tissue surface, with a silicon stop over the gingival surface.
Time Frame
18 months
Title
peri-implant gingival index
Description
Periodontal probe was used to measure 6 sites on buccal and lingual side each time to observe gingival color, texture and bleeding, and record the scores.
Time Frame
18 months
Title
peri-implant gingival recession
Description
The distance between the implant shoulder and the gingival margin of the temporary or final crown was measured with a periodontal probe (only when the implant shoulder was visible).
Time Frame
18 months
Title
visual analogue scale
Description
Visual analogous scale ( VAS) suggested by WHO was used to assess. Analgesia intensity expressed with 0-10, 0 point as without pain completely, 10 points as unbearable pain.
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
No systemic diseases or pregnancy;
The thickness of keratinized mucosa where the posterior tooth is missing is less than 2 mm;
Full-mouth plaque score (FMPS) < 20% (measured at four sites per tooth) and bleeding on probing score (BOP%) ≤25% (measured at six sites per tooth);
Periodontal condition is stable, no probing depths ≥5 mm;
No previous soft tissue augmentation procedure at experimental site;
The patient has signed informed consent and accepts the operation of subepithelial connective tissue transplantation.
Exclusion Criteria:
Patients with uncontrolled hypertension;
Patients with uncontrolled diabetes;
Patients with insufficient oral hygiene and Untreated periodontitis;
Pregnant or lactating women;
Smoker;
Patients with long-term (> 6 months) use of glucocorticoids;
History of malignancy, radiotherapy, or chemotherapy for malignancy within the past 5 years;
Patients with severe cardiovascular problems;
Patients with uncontrolled infectious or metabolic diseases;
Patients with substance abuse.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Weilian Sun, PhD
Phone
13757119563
Email
weiliansun@zju.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Weilian Sun
Organizational Affiliation
Second Affiliated Hospital, School of Medicine, Zhejiang University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Oral Medicine, the Second Affiliated Hospital, School of Medicine Zhejiang University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310009
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Weilian Sun
12. IPD Sharing Statement
Plan to Share IPD
No
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Increased Peri-implant Keratinized Mucosal Thickness at Different Operative Times
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