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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06193460
Other study ID # ODHOD-101-1Q
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 1, 2024
Est. completion date June 1, 2024

Study information

Verified date January 2024
Source Al-Azhar University
Contact Alaa Eldehna, M.D
Phone +201068837641
Email alaaaldehna.26@azhar.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate the effect of the photobiomodulation mode of the diode laser on the anaesthetic area and find the best parameter that would accelerate the withdrawal of anaesthesia.


Description:

A randomized clinical trial will be performed at the Pedodontics Out Paediatric Clinic at the Facility of Dental Medical for girls. Al Azhar University has twenty patients with upper or lower first primary molars on the right and left sides that need to be treated. Using the split-mouth technique, the mouth will be split in two halves. The first half represents the first group, and the second half represents the second group. Group I (20 teeth): the anaesthesia will be reversed by the photobiomodulation mode of diode laser (low-level laser therapy). Group II (controlled group): 20 teeth of anesthesia will be withdrawn without intervention. To avoid bias in the 2nd group, the laser will be applied on this side, but in turned-off mode. The type of anaesthesia that will be evaluated is articine hydrochloride 4% with 1:200 epinephrine (vasoconstrictor).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date June 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 12 Years
Eligibility Inclusion Criteria: Parents have to complete the written consent form. Patient who behaved well. Children aged from 6 to 12 years can evaluate soft tissue anaesthesia. Patients that require treatment with bilateral upper or lower first primary molar infiltration under anaesthesia. Exclusion Criteria: Patients who are mentally disordered or hand-capped. uncooperative patients.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
low-level laser therapy
photobiomodulation mode of diode laser (low-level laser therapy).

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Al-Azhar University

Outcome

Type Measure Description Time frame Safety issue
Primary Outcomes measuring the duration (in minutes) of anaesthesia withdrawal after laser application Return the normal sensation to the lip.
Being able to smile, drink, and talk normally.
Return of pain sensation that result from the procedure
after application of laser immediately and continue each 15 minutes till complete withdrawal of anaesthesia
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