Evaluation of a New Technique for Periodontal Pocket Reduction in the Extraction of Wisdom Teeth

The study population will be the patients of the University Clinic of the Rey Juan Carlos University of Madrid.

A non-probabilistic selection method will be used in the Master's Degree in Periodontology and Osseointegration and the Integrated Adult Clinical Dentistry course, for those patients who meet the inclusion criteria for the study.

Patients will be assigned to the experimental and control groups by probabilistic methods using a table of random numbers.

Variables:

Independent Variable: Surgical technique. In the experimental group, the Distal Reduction Flap (DRF) technique and primary wound closure will be used. In the control group, the conventional exodontic technique and secondary wound closure will be used.

Dependent variables. The reduction of probing depth at 6 weeks (RPS6) and 18 weeks (RPS18) will be evaluated. Modifying variables: The contribution of the following socioeconomic variables will be assessed:

Sex (male, female) Age (years) Systemic Diseases (Yes, No) Medication (Specify which) Tobacco (Yes, No) Mechanical Dental Plaque Control (Manual Brushing, Electric Brushing, or both) Chemical Dental Plaque Control (Yes, No)

The sequence of work:

T.0: A first consultation "Interview" will be carried out in which the nature of the study will be explained to the patient. A check will be made to see if the patient meets the inclusion criteria to take part in the study.

Periodontal probing with a Hu-Friedy® CP15 probe with 1 mm markings with a range of 0 to 15 mm. There will be a periodontal pocket distal to the second molars (probing depth equal to or greater than 4 mm).

• The patient must be periodontally stable: Periodontal probing equal to or less than 4 mm and with bleeding on probing (BOP) index less than 25%.

• Measure the amount of keratinized gingiva on vestibular and lingual/palatal second molars with a Hu-Friedy® CP15 periodontal probe, measuring the distance between the gingival margin and the amelo-cement line. There will be a minimum of 3 mm, to make a 1 mm buckle and keep at least a 2 mm band remaining.

• Photographic records with Nikon®D5200 digital SLR camera body, with Nikon® compatible Sigma® 50 mm macro lens, Meke® ring flash, side mirror, and lip retractors.

T.1: On the day of surgery the working procedure will consist of:

• Anesthetic technique will be performed with infiltrative injection if it is in the upper jaw for blockade of the Posterior Alveolar Nerve and Palatine Nerve Major and Minor, and if it is in the lower jaw, regional injection will be performed for blockade of the Inferior Dental Nerve, Lingual Nerve and infiltrative for blockade of the Buccal Nerve. With Articaine 4% with epinephrine at 1:100.000. Ultracain ® (Normon® Laboratories, Madrid, Spain).
• The intervention will be performed according to the assigned randomization.

T.2: A review will be performed after 14 days and a photographic record will be taken, together with suture removal in the case of the study group. Post-operative discomfort perceived by the patient during the 3 days following the intervention will be recorded using V.A.E.

T.3: A review will be carried out 6 weeks after the intervention, where in addition to a photographic record, periodontal probing will be repeated with a Hu-Friedy® CP15 probe in the distal part of the 2nd molar. The reduction, persistence, or increase of the pre-existing periodontal pocket will be assessed.

T.4: A check-up will be performed at 12 weeks (18 weeks after the intervention). A new periodontal probing with a Hu-Friedy® CP15 probe in the distal part of the 2nd molar and a new photographic record will be taken.

Inclusion criteria

• Patients who require third molar extraction and who have periodontal pockets distal to the adjacent second molars.
• In the second molars there should be enough keratinized gingiva to allow for a buccal and/or lingual-palatal buckle (minimum residual band of 2 mm).
• Patients of either sex.
• Patients over 18 years old.
• Healthy patients or in a controlled periodontal situation (previously treated with basic periodontal therapy with scaling and root planing with probing depths of less than 4 mm and bleeding index at probing <25%).
• In the case of pharmacologically treated patients, they should be properly controlled and request prior consultation to evaluate pharmacological treatments that may lead to hematological alterations.

Exclusion criteria

• Patients with uncontrolled pathologies or systemic conditions.