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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05748223
Other study ID # Cukurova U
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 20, 2022
Est. completion date January 13, 2023

Study information

Verified date February 2023
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this pioneer study was to evaluate the efficacy (heart rate value, blood pressure, oxygen saturation, cortisol levels, BIS monitoring, patients' anxiety) of Mindfulness Meditation as a sedative technique during dental implant surgery.


Description:

Since anxiety is a form of psychological stress, an increase in anxiety results in a surge in stress levels. The role of sedation in dental surgery cannot be overemphasised. The reduction in pain and anxiety eventually causes better cooperation and patients' satisfaction. Therefore, balancing anxiety and/or stress levels in patients would be useful to ensure patient safety during treatment.Therefore, the aim of this pioneer study was to evaluate the efficacy (heart rate value, blood pressure, oxygen saturation, cortisol levels, BIS monitoring, patients' anxiety) of Mindfulness Meditation as a sedative technique during dental implant surgery.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date January 13, 2023
Est. primary completion date November 11, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 65 Years
Eligibility . The inclusion criteria were: - age between 25-65 years-old - single tooth loss in the maxillary premolar-molar region with partial bone healing (type 3) or fully healed ridge type 4 - sufficient bony ridge for implant placement without the need for simultaneous bone grafting or sinus lift procedure - no signs of acute oral infection, - more than 2 mm of keratinized gingiva at the site of surgery - periodontally healthy (or successfully treated) and otherwise healthy or had well-controlled systemic disease (ASA classification I, II). Exclusion criteria were - diabetes mellitus - smoking - pregnancy; - diagnosis of anxiety disorders/psychiatric disorder/ depression and whether or not they were seeking any form of treatment for these conditions; - poor oral hygiene (plaque control record > 30%); - history of radiation therapy at head and neck area and chemotherapy; bony pathologies; history of soft tissue grafting at the prospective implant site

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mindfulness Meditation
Mindfulness meditation has been reported to produce beneficial effects on a number of psychiatric, functional somatic, and stress-related symptoms and has therefore increasingly been incorporated into psychotherapeutic programs

Locations

Country Name City State
Turkey Cukurova University Faculty of Dentistry Adana

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Bispectral Index (BIS) monitoring The level of sedation achieved by meditation was assessed with BIS device. BIS values range between 100 and 0 and give the clinicians objective information about the depth of sedation. Change from baseline to 5th, 10th, 15th, 20th, 25th and 30th minutes
Secondary Cortisol The cortisol levels were biochemically evaluated At the baseline, immediately before and 5-minutes after surgery for both groups.
Secondary Blood pressure systolic and diastolic blood pressure (in mmHg) via vital signs monitor for both groups Every 5-minutes starting from baseline until the end of surgery for both groups
Secondary arterial blood oxygen saturation in 'percentage %' via vital signs monitor for both groups Every 5-minutes starting from baseline until the end of surgery for both groups
Secondary heart rate value in 'beats per minute' via vital signs monitor for both groups Every 5-minutes starting from baseline until the end of surgery for both groups
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