Health TrialsbyHealthPanel

Buccal Infiltration of Different Volumes of Articaine for Extraction.

ConditionsBuccal InfiltrationArticaineAnesthesia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorQassim University

About this trial

This study compares the effectiveness of two different volumes of buccal infiltration of Articaine for the extraction of mandibular posterior teeth. One group receives buccal infiltration of 1.8 ml of 4% Articaine and the other group receives buccal infiltration of 3.6 ml of 4% Articaine.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

All healthy patients (ASA I) or patients with mild systemic disease with no functional limitations (ASA II)

Patients aged ≥ 18 years of age.

Patients requiring extraction of mandibular posterior teeth including grossly decayed tooth, grade I mobile tooth, root stumps and indicated for therapeutic reasons.

Patients not allergic to the drugs or anesthetic agents used in the surgery.

Disqualifiers

Acute infection at the extraction site.

Patients indicated for surgical extraction of teeth.

Patients already taking medications affecting pain assessment.

Pregnant patients.

Trial design

Design model

Parallel

Treatments tested in this trial

  • 1.8 ml of 4% Articaine

    Other intervention

    Buccal infiltration of 1.8 ml of 4% Articaine

  • 3.6 ml of 4% Articaine

    Other intervention

    Buccal infiltration of 3.6 ml of 4% Articaine.

Treatment groups

114 Participants
are divided into 2 treatment groups
Group A: Group AExperimental treatment 1 intervention
Group B: Group BActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Intensity of pain

VAS scale is a validated scale measuring pain with possible score range from 0 (no pain) to 100 (severe pain).

Time frame
From reflection of mucoperiosteum till delivery of tooth out of socket.
2

Time of onset of anesthesia

It will be assessed by probing buccal and lingual soft tissue using a dental explorer every 2 minutes after infiltration using a standard digital stop clock.

Time frame
upto 10 minutes
3

Presence or absence of pain

A 100 mm Numerical rating scale assessing intraoperative pain. Possible score ranges from 0 (no pain) to 100 (worst possible pain).

Time frame
From reflection of mucoperiosteum till delivery of tooth out of socket.

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Qassim University

Lead sponsor

Source ClinicalTrials.gov
Apply now