Clinical TrialID 5841

Non Surgical Treatment of Periimplantitis

NCT02023853

Peri-Implantitis and Peri-implant Mucositis

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5841
Evidence Id
5841
Core Evidence Id
5841
Source Clinical Trial Id
5825
Herb2 Clinical Trial Id
HBCT005825
Nct Id
NCT02023853
Title
Non Surgical Treatment of Periimplantitis
Status
Completed
Phase
Phase 4
Study Result
No
Study Condition
Peri-Implantitis and Peri-implant Mucositis
Study Type
Interventional
Study Design
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
PROCEDURE: ultrasonic|PROCEDURE: erythritol|DRUG: metronidazole gel
Intervention Allocation
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
20
Outcome Measure
probing pocket depth change, baseline, 6 months|bleeding on probing change, baseline, 6 months|clinical attachment level change, baseline, 6 months
Sponsor Collaborator
Proed, Torino, Italy
Funded By
OTHER
Location
PROED, Institute for Professional Education in Dentistry, Torino, 10129, Italy
Other Id
Proed.08.2013.periimplantitis
Start Date
2013-12
Primary Completion Date
2015-02
Completion Date
2015-12
First Posted
2013-12-30
Results First Posted
Last Update Posted
2016-09-02
Study Document
Study Url
https://clinicaltrials.gov/study/NCT02023853
Title Cn
Title En
Non Surgical Treatment of Periimplantitis
Bilingual Status
semi_complete