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Recruiting NCT06808373

The Effect of Hypnosis on Periodontal Treatment

No phase Interventional Peridontal Disease Dental Anxiety

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: hypnosis.
Who it may be relevant to
Registry conditions: Peridontal Disease, Dental Anxiety. Basic parameters: 20 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Hypnosis on Healing in Patients Undergoing Phase I Periodontal Therapy

Overview

Treatment of periodontal diseases relies on the mechanical removal of microbial dental plaque, calculus, and necrotic cementum from root surfaces in both supra- and subgingival areas to control inflammation in periodontal tissues. As in all dental treatments, dental phobia and dental anxiety are common challenges in initial periodontal therapy. Hypnosis is among the traditional non-pharmacological behavior management techniques used to manage stress and improve pain tolerance. It is known that hypnosis is effective in anxiety control in dentistry. The use of salivary levels of inflammatory mediators released during the disease is a valid method for assessing the progression of periodontal disease and healing after treatment. In this study, the effect of hypnosis on healing in patients undergoing Phase I periodontal therapy will be evaluated by comparing the mean differences in cytokine levels between case and control groups

Interventions

  • Behavioral hypnosis
    Hypnosis will be applied to periodontitis patients

Primary outcome measures

  • measurement of cytokine levels [Time frame: Pre-treatment (day 0), post-treatment (day 0) and 8 weeks post-treatment]

Eligibility criteria

Inclusion criteria

Being between the ages of 20-65 Not having any systemic disease Having chronic periodontal disease Having the ability to understand the study and answer questions

Exclusion criteria

Having any systemic disease Being under 20 or over 65 Not having any periodontal disease

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Afyonkarahisar Health Sciences University Faculty of Dentistry — Afyonkarahisar

Identifiers

NCT: NCT06808373 · SBUSAH-GETAT 2024-054

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗