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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05140681
Other study ID # FibReORSTurin
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2017
Est. completion date December 23, 2018

Study information

Verified date November 2021
Source University of Turin, Italy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is lack of data in literature on keratinized tissue increase after FibReORS in relation to primary flap position. This study has been designed as a split-mouth randomized trial to assess the influence of flap position after FibReORS. 16 patients were recruited and treated. The placement of the flap 2 mm apically to the bone crest instead at the bone level would be a viable approach to increase KT width without delaying wound healing. The extent of post-operative discomfort/pain was not influenced by primary flap position.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 23, 2018
Est. primary completion date October 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1) diagnosis of severe chronic periodontitis (corresponding to grade III or IV according to the actual classification); 2) good general health; 3) full-mouth plaque score (FMPS) and full-mouth bleeding score (FMBS) < 20%; 4) at least two contralateral sextants with residual PDs of > 5 mm and persisting bleeding on probing (BoP) at posterior natural teeth 3 months after the completion of cause-related therapy Exclusion Criteria: 1) pregnancy and lactation; 2) smoking > 10 cigarettes/day; 3) intake of antibiotics in the previous 6 months. In addition, teeth with degree II or III mobility, horizontal bone loss higher than 1/3 of the root length or designed as abutment for prosthetic rehabilitation were also excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
FibReORS with apically positioned flap (apical position)
Periodontal surgery including flap elevation. root surface scaling, bone remodeling and suture of the flap at 2 mm subcrestal position
FibReORS with apically positioned flap (crestal position)
Periodontal surgery including flap elevation. root surface scaling, bone remodeling and suture of the flap at either a crestal position

Locations

Country Name City State
Italy C.I.R. Dental School. Università di Torino Torino TO

Sponsors (1)

Lead Sponsor Collaborator
University of Turin, Italy

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Amount of soft tissue re-growth after FibReORS The amount of regrowth is calculated from the position of the tissue at the end of the surgery 6 months
Secondary Amount of KT increase after FibReORS The amount of KT increase is calculated from the position of the tissue at the end of the surgery 6 months
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