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Evaluation of Behavioral Feedback of 6-10 Years pediatric dental pateints by Using Virtual Reality Technique during Pulpotomy of Primary molar teeth

The Impact of Virtual Reality Technique on level of Pain and Anxiety during Pulpotomy of Primary molar teeth

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014122420413N1
Enrollment
20
Registered
2015-01-31
Start date
2014-12-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: situational anxiety. Condition 2: pain(tooth pain). Other childhood emotional disorders Other specified disorders of teeth and supporting structures

Interventions

Intervention 1: The intervention group: during Local Anesthesia injection and Pulpotomy used an audiovisual eye glasses system (Model: 3D X-Mage VG 601) with internal memory and showed TOM & GERRY car
Behavior
The intervention group: during Local Anesthesia injection and Pulpotomy used an audiovisual eye glasses system (Model: 3D X-Mage VG 601) with internal memory and showed TOM & GERRY cartoon that It is
The control group: underwent injection with no intervention during Pulpotomy

Sponsors

Deputy of Research of Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 6-10 years old children;The Existence of two carious primary molars (D or E) in the maxilla or mandible necessitating Pulpotomy;Not to have Unpleasant Not to have experiences in medical settings; Not to have Any experience in dental treatment, audiovisual disorders; Not to have Mental and physical disorders; Not to have Childhood anxiety related disorders; Not to have Allergies to Lidocain. Exclusion criteria: Toxic children; Treatment time which lasts more than 30 minutes If the patient needs more than one anesthesia; Children who have gag reflex;Children who need pulpectomy during treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Systolic and diastolic Blood Pressure and Hart Rate. Timepoint: Before and After pulpotomy. Method of measurement: Pediatric Blood Pressure Monitor with Cuff.;Pain. Timepoint: before and after pulpotomy. Method of measurement: Wong-Baker Fasces Pain Rating and frankle scale.;Child’s behavior. Timepoint: before and after pulpotomy. Method of measurement: Frankle scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNegar mohammadi

Faculty od dentistry, Qazvin University of Medical sciences

mohamadinegar@yahoo.com+98 86 4633 0979

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026