Comparison of Dental Pain Response in Children

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-01

Study Completion Date

2023-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Study involves the observation of the child's behavior during a dental treatment procedure. This allows for the evaluation of the child's experience of pain and discomfort through their facial expressions, body movements, and vocalizations during the procedure.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Comparison of Effectiveness of Pre-cooling With Ethyl Chloride Versus Honey

NCT05568563

Irreversible Pulpitis

COMPLETED NA

Emotional and Oral Characteristics of Patients That Attend a Dental Consultation for the Extraction of Third Molars

NCT06388265

Anxiety and Fear

COMPLETED NA

Pain Perception: on Relationships Between Dental Anxiety and Olfaction

NCT05369936

Dental Anxiety Dental Pain Essential Oil

COMPLETED NA

Postoperative Pain in Children Aged From 3 to 5 Years Following Full Mouth Dental Rehabilitation Under General Anesthesia. A Cross-sectional Study. Rehabilitation Under General Anesthesia

NCT03739567

Post-operative Pain

UNKNOWN

The Effect of Cartoon and Music Applications on Dental Pain

NCT07336719

Pain Management Dental Anxiety Distraction +1 more

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dental Anxiety

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

behaviour

Group Type EXPERIMENTAL

experimental

Intervention Type BEHAVIORAL

During the procedure, the chairside assistant can capture video recordings of the child's behavior and facial expressions. These videos can be later reviewed by a trained observer who can evaluate the child's pain experience

control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

experimental

During the procedure, the chairside assistant can capture video recordings of the child's behavior and facial expressions. These videos can be later reviewed by a trained observer who can evaluate the child's pain experience

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age range: Children aged between 6-12 years old (or any other specific age range) will be included in the study.
* Dental pain: Participants who have been diagnosed with dental pain by their dentist will be included.
* Consent: Informed consent must be obtained from the child and their parents or guardians before the study.

Exclusion Criteria

* Participants with existing medical or psychological conditions that could affect the pain response for instance, children with chronic pain conditions or with a history of anxiety or depression.
* Participants who have taken any pain medication within the past 24 hours as this could interfere with the pain response.

Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes