Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03844035
Other study ID # B.30.2.ODM.0.20.08/1034
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 6, 2014
Est. completion date June 5, 2015

Study information

Verified date February 2019
Source Ondokuz Mayis University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study aimed to investigate clinically the cleaning effectiveness of different treatment modalities, that is, oral irrigator or interdental brush usage addition to routine brushing and examine TGF-β1, IL-1β, t-PA, and PAI-1 levels in periimplant crevicular fluid of patients with periimplant mucositis. The null hypothesis was that oral irrigators would be effective compared to interdental brush in the oral care of individuals who use implant-supported protheses.


Description:

Detailed Description: Our aim was to evaluate efficacy of a manual tooth-brush with either interdental brush or oral irrigator in treatment of periimplant mucositis.

Material and Method: Forty-five patients with periimplant mucositis having at least one implant (age range:45-60) were included in study. Study was planned as randomized, single-blind, parallel-design. Patients were divided into 3 equal groups; i)toothbrush+oral irrigator ii)toothbrush+interdental brush, iii)only toothbrush. After baseline examinations [Silness-Löe plaque index(PI), Löe-Silness gingival index(GI), probing pocket depth(PPD), clinical attachment level(CAL), bleeding on probing(BOP)], initial periodontal therapy was completed using full-mouth disinfection method. Periimplant crevicular fluid(PCF) were taken from patents to assess levels of interleukin-1beta(IL-1β), Transforming growth factor-beta(TGF- β), tissue-type plasminogen activator(t-PA), plasminogen activator inhibitor-1(PAI-1). Clinical records were repeated at 2, 4 and 12 weeks.

The hypothesis of our study is that oral irrigators may be effective in oral care of individuals using an implant-supported prosthesis because of the ease of use.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date June 5, 2015
Est. primary completion date May 4, 2015
Accepts healthy volunteers No
Gender All
Age group 45 Years to 60 Years
Eligibility Inclusion Criteria:

- subject with no systemic diseases that affect oral tissues and the nature of plaque,

- with no professional cleaning for at least six months prior to baseline examination,

- with one or more implants (Straumann, Waldenburg, Switzerland) functioning at least 24 months before the start of the study

- having implants with BOP in at least two of the six regions

- The people who agreed to refrain from the use of any nonstudy dental device or oral care product for the study duration were included in the study

Exclusion Criteria:

Exclusion criteria

- subjects not cooperative,

- having disease associated with bacteremia,

- taking medication influencing gingival health (eg. dilantin, calcium channel blockers, cyclosporine, anticoagulants),

- using long-term antibiotic and anti-inflammatory agents,

- smokers and

- women who were pregnant and in lactation period

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Periimplant crevicular fluid (PICF) collection
Prior to PICF sampling, supragingival plaque was removed by sterile curets and, after air drying, the surfaces were isolated by cotton rolls. Filter paper strips (periopaper, proflow Inc., Amityville, New York, USA) were placed in sulcus for 30s. Care was taken not to avoid mechanical trauma and strips contaminated with blood or saliva were discarded. The absorbed PICF volume was estimated by a calibrated instrument (periotron 8000, proflow Inc., Amityville, NY, USA). Then, the strips were sealed into sterile tubes before freezing at -80°C. The readings were converted to an actual volume (µl) by reference to the standard curve.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ondokuz Mayis University

Outcome

Type Measure Description Time frame Safety issue
Primary Periimplant crevicular fluid level of IL-1ß as a marker of gingival inflammation Elevated levels of IL-1ß in periimplant crevicular fluid have been associated with the destructive changes that occur in the inflamed human gingiva through study completion, an average of 1 year
Primary Periimplant crevicular fluid level of TGF-ß1 as a marker both of inflammatory phase and proliferative phase TGF-ß1 plays a role in the development and progression of periodontal diseases. through study completion, an average of 1 year
Primary Periimplant crevicular fluid level of t-PA as a marker for clinical evaluation and efficacy of periodontal treatment Higher levels of t-PA in periimplant crevicular fluid have been associated with gingivitis and periodontitis. through study completion, an average of 1 year
Primary Periimplant crevicular fluid level of PAI-1 as a marker for clinical evaluation and efficacy of periodontal treatment Higher levels of PAI-1 may be associated with progression of periodontitis through study completion, an average of 1 year
See also
  Status Clinical Trial Phase
Completed NCT05332327 - Comparison of the Accuracy of Different Periodontal Probes for Peri-implant Pocket Registration
Enrolling by invitation NCT06063876 - Experimental Peri-implant Mucositis on Implant Sites That Were Previously Treated With or Without Implantoplasty N/A
Completed NCT01941797 - Experimental Peri-implant Mucositis in Humans N/A
Enrolling by invitation NCT05675241 - Characterizing the Inflammation Around Dental Implants
Completed NCT04874467 - Influence of Keratinized Mucosa on Dental Implants With Mucositis N/A
Recruiting NCT05906810 - Impact of Non-surgical Periodontal Therapy in the Improvement of Early Endothelial Dysfunction in Subjects With Peri-implantitis and Peri-implant Mucositis N/A
Enrolling by invitation NCT06137846 - Treatment of Peri-implant Mucositis and Supportive Peri-implant Therapy N/A
Completed NCT05945836 - Peri-implant Disease and Prosthetic Cement: Cross-sectional Study
Not yet recruiting NCT05897736 - Salivary Minerals in Patients With Peri-implantitis
Recruiting NCT04052373 - Peri-implantitis Implantoplasty Treatment N/A
Completed NCT03533166 - Effects of a 0.03% CHX Mouth Rinse in Peri-implant Mucositis N/A
Completed NCT03693196 - The Effect of Different Dental Implant Surface Characteristics on Immunological and Microbiological Parameters N/A
Completed NCT03421717 - The Effect of Peri-implant Surgery and Chair-side Supportive Post Surgical Peri-implant Therapy N/A
Completed NCT03998865 - Bacterial Microbiota Characterization on Implant-supported PEEK and Titanium Provisional Abutments N/A
Recruiting NCT05592314 - Lnfluence of the Prosthetic Emergence Profile on the Prevalence of Peri-implant Diseases: a Cross Sectional Study
Completed NCT04899986 - Chlorhexidine Gel and Peribioma Periogel Use in Peri-implant Mucositis Sites: a Split-mouth Randomized Clinical Trial. N/A
Recruiting NCT04415801 - Effect of Repeated Removal and Re-placement of Abutments Around Dental Implants N/A
Recruiting NCT04283903 - Metabolomic and Proteomic Fingerprinting in Peri-implant Diseases
Completed NCT04215432 - Propolis Extract, Nanovitamin C and Nanovitamin E in Peri-implant Mucositis N/A
Active, not recruiting NCT05834946 - Biological Responses Affecting Early-stage Dental Implant Placement in Patients With History of Periodontitis N/A