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Completed

NCT Number: NCT05472233

Effect of Suturing Protocols on Coronally Advanced Flap for Root Coverage Outcomes

The purpose of this retrospective study is to investigate whether suturing protocols (suture removal timing) influence root coverage outcomes in recession defects treated with a coronally advanced flap (CAF) procedure.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Policlinico Duilio Casula, AOU Cagliari

Monserrato, CA, 09042, Italy

About this study

The aim of this study is to assess whether the timing of suture removal may influence the number of sites exhibiting complete coverage (CRC) or the mean root coverage (MRC) obtained in single-tooth recession-type defects treated by coronally advanced flap (CAF).

Records from patients that underwent a coronally advanced flap (CAF) procedure for root coverage will be analyzed. This surgical procedure is aimed at the treatment of root recessions that may arise following periodontal disease or mechanical trauma. The procedure, after obtaining deep local anesthesia, involves a sulcular incision on the buccal side and extending the incision mesially and distally to the base of the adjacent papillae. Two vertical incisions are then made at the corner of the adjacent tooth line and extended into the alveolar mucosa. A mixed thickness flap is then elevated and coronally advanced by releasing incisions through the periosteum to allow for flap placement to cover the recession without tension. The papillae are de-epithelized to provide the bed of connective tissue for the adaptation of the flap which is then sutured with single stitches.

The records, complete with photographic documentation, of all patients who have undergone this procedure will be identified and will be divided into two groups: those in which the sutures were removed at 2 weeks and those in which the sutures were removed at 3 or more weeks.

CRC as present or absent (yes/no) and MRC (percentage of roof surface that has been successfully covered) six months after surgery will be assessed in these patients.

The presence of patient discomfort on the day of suture removal will be recorded as present / absent to assess whether the permanence of the sutures for longer or shorter influences the patient's perception of the surgery.

The results will be compared between the two groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients not affected by active periodontitis
  • Single recessions on non-restored non-molar teeth
  • CAF protocols using vertical releasing incisions
  • records of patients clearly reporting timing of suture removals and root coverage outcomes at 6 months

Exclusion criteria

  • Adjacent recessions
  • Recessions on molar teeth
  • Coronally advanced flaps without releasing incisions
  • Patients with active periodontitis

Treatment and study plan

Suture removal after Coronally Positioned Flap

Procedure

Sutures are removed after different healing period post coronally positioned flap surgery, this latter is a procedure that aims at surgically advancing the gingiva in order to cover dehiscences of the soft tissues uncovering dental roots.

Primary outcomes

  1. Complete Root Coverage

    Time frame: 6 months

    Achievement of 100% root coverage, measured as yes / no

  2. Mean Root Coverage

    Time frame: 6 months

    Percentage of the root recession that has been successfully covered after the surgical procedure

Secondary outcomes

  1. Patient discomfort

    Time frame: at suture removal

    Discomfort reported by the patient (present/absent)

Sponsors and collaborators

Lead sponsor

University of Cagliari

Other

Registry information

Official study title

The Effect of Sutures Removal Protocols on Coronally Advanced Flap for Root Coverage Outcomes: a Retrospective Study

Important dates

Study start
2022
Primary completion
2022
Study completion
2025
First posted
Jul 25, 2022
Registry last updated
Jul 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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