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The Use of Water Jet for Initial Treatment FOR Peri-Implant Disease

This study is currently recruiting participants.
Verified September 2017 by Rambam Health Care Campus
Sponsor:
ClinicalTrials.gov Identifier:
NCT01509898
First Posted: January 13, 2012
Last Update Posted: September 29, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
Rambam Health Care Campus
  Purpose
The aim of this study was to evaluate the effect of a dental water jet on initial peri-implant disease resolution.

Condition Intervention
Peri-implantitis Device: Water jet

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: The Use of Water Jet for Initial Treatment FOR Peri-Implant Disease

Resource links provided by NLM:


Further study details as provided by Rambam Health Care Campus:

Primary Outcome Measures:
  • Probing depth [ Time Frame: one month ]
    Probing depth around the implant


Secondary Outcome Measures:
  • Bleeding on probing [ Time Frame: one month ]
    Bleeding on probing (BOP) around the implant


Estimated Enrollment: 40
Actual Study Start Date: July 18, 2012
Estimated Study Completion Date: November 2018
Estimated Primary Completion Date: November 2018 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: water-Jet
use of water jet for 1 month
Device: Water jet
use of water jet for a month
Other Name: silonit water jet

Detailed Description:
Peri-implant disease is becoming more frequent during the last decade. Till today, there is no effective evidence-based treatment. The use of water-jet might improve those situations and reduce morbidity and implant loss.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Signed and dated Informed Consent Form.
  • Patient suffer from peri- implant disease
  • Age Eligible for study: 18 year old and older
  • Genders Eligible for study: Both

Exclusion Criteria:

  • Patient substantially fails to comply with the study schedule, or treatment program as described in this Protocol.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01509898


Contacts
Contact: Dr. liran Levin, DMD +972502062820 l_levin@rambam.health.gov.il

Locations
Israel
Rambam Hospital Recruiting
Haifa, Israel
Contact: Dr. Liran levin, DMD    972    l_levin@rambam.health.gov.il   
Sponsors and Collaborators
Rambam Health Care Campus
Investigators
Study Director: Dr. Liran Levin, DMD Department of periodontology
  More Information

Responsible Party: Rambam Health Care Campus
ClinicalTrials.gov Identifier: NCT01509898     History of Changes
Other Study ID Numbers: 0374-11-RMB
First Submitted: January 1, 2012
First Posted: January 13, 2012
Last Update Posted: September 29, 2017
Last Verified: September 2017

Additional relevant MeSH terms:
Peri-Implantitis
Periodontal Diseases
Mouth Diseases
Stomatognathic Diseases