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Surgical Treatment of Gingival Recessions

M

Medipol Health Group

Status

Completed

Conditions

Microsurgery
Gingival Recession
Clinical Trial
Connective Tissue

Treatments

Procedure: surgical techniques in the treatment of localized gingival recession defects.

Study type

Interventional

Funder types

Other

Identifiers

NCT04611282
Mamtograrct

Details and patient eligibility

About

The purpose of this study was to compare the effectiveness of microsurgical and macrosurgical approaches on CPFs plus SCTGs for the treatment of localized gingival recession defects (Miller class I or II) over the course of 6 months based on clinical periodontal parameters, periodontal phenotypes, and the postoperative complaints and satisfaction levels of the patients. We hypothesized that root coverage achieved through microsurgery in Miller I or II gingival recessions would improve clinical periodontal outcomes and the periodontal phenotype, with greater postoperative comfort and aesthetic satisfaction in comparison with conventional macrosurgical techniques. Miller Class I and II gingival recession defects, at least 3.0 mm deep, were selected and randomly assigned to receive micro or macrosurgical techniques. Both techniques were performed using a coronally positioned flap with a subepithelial connective tissue graft. Plaque and gingival indices, gingival recession depth and width, probing pocket depth, bleeding on probing, clinical attachment level, width of keratinized gingiva, aesthetic score and percentage of root coverage, postoperative complaints, and satisfaction of the participants completing the study were evaluated at follow-up 1st, 3rd and 6th months.

Enrollment

17 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

All participants were:

  • adults aged 18 years or over
  • systemically and periodontally healthy
  • met the eligibility criteria for localized gingival recession of the canine or premolar teeth according to the Miller classification scheme

Exclusion criteria

Exclusion criteria included the following:

  • medical disorders such as diabetes mellitus, immunologic disorders, and hepatitis;
  • a history of chemotherapy or radiotherapy;
  • a history of alcoholism or drug abuse;
  • a history of previous mucogingival surgery at the gingival recession site;
  • medications known to affect gingival tissues;
  • antibiotic treatment in the past 6 months;
  • smoking >10 cigarettes per day for >5 years, and;
  • current pregnancy or lactation.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

17 participants in 2 patient groups

Microsurgery group
Experimental group
Description:
All defects were treated with a CPF plus an SCTG by the same investigator using microsurgery technique.
Treatment:
Procedure: surgical techniques in the treatment of localized gingival recession defects.
Macrosurgery group
Active Comparator group
Description:
All defects were treated with a CPF plus an SCTG by the same investigator using macrosurgery technique.
Treatment:
Procedure: surgical techniques in the treatment of localized gingival recession defects.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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