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Compares treatment options for Irreversible Pulpitis with Apical Periodontitis
Official title The Effect of Eddy Sonic Versus AF Max Activation of Bio-ceramic Sealer on Post-operative Pain in Teeth with Symptomatic Irreversible Pulpitis with Apical Periodontitis
ClinicalTrials.gov ID: NCT06640218
What this study is testing
- What it's testing
- The aim of endodontic therapy for an inflamed tooth is to eliminate the source of inflammation. Relieving pain depends on the effectiveness of root canal therapy.3 Postoperative pain in endodontic treatments, affecting 3-58% of patients, is often caused by peri-radicular tissue injuries.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 40. Healthy volunteers may be eligible.
You may be able to join if
- Age range is from 18 to 40 years old.
- No sex predilection
- Patients seeking root canal treatment.
- restorable teeth.
- Positive patient acceptance for participating in the study.
You likely can't join if
- Patients with American Association of Anesthesiologists (ASA) classifications other than ASA 1 \& Il
- Patients who have already ingested preoperative medication, such as analgesics, non-steroidal, or steroidal anti-inflammatory drugs, within 12 hours...
- This was done to prevent any misinterpretation of the diagnosis or post-treatment pain severity, as these drugs substantially lower post-endodontic...
- Patients with NSAID allergy.
- Patients having two or more adjacent teeth needing root canal therapy
- Pregnant patients.
See the full eligibility criteria
- Age range is from 18 to 40 years old.
- No sex predilection
- Patients seeking root canal treatment.
- restorable teeth.
- Positive patient acceptance for participating in the study.
- patients able to sign informed consent.
- Systematically healthy patient (ASA I, Il).
- Patient who can understand the numerical rate scale and sign an informed consent.
- Mandibular first molar teeth with pain on bite or percussion
- Preoperative sharp (moderate or severe) pain.
- Vital response of pulp tissue to cold pulp tester (ethyl chloride spray).
- widening in periodontal membrane space in radiographic appearance.
- Patients with American Association of Anesthesiologists (ASA) classifications other than ASA 1 \& Il
- Patients who have already ingested preoperative medication, such as analgesics, non-steroidal, or steroidal anti-inflammatory drugs, within 12 hours of the start of treatment.
- This was done to prevent any misinterpretation of the diagnosis or post-treatment pain severity, as these drugs substantially lower post-endodontic pain (Jorge-Arajo et al.,2018).
- Patients with NSAID allergy.
- Patients having two or more adjacent teeth needing root canal therapy
- Pregnant patients.
- Patients with bleeding disorder.
- Patients with long-term corticosteroid use.
- Teeth having:
- Necrotic pulp.
- History or presence of swelling or fistulous tract.
- Acute/chronic periapical abscess.
- Mobility more than grade 1.
- Pocket depth of more than 5mm
- No possible restorability.
- Previous root canal treatment.
- Periapical radiolucency.
- External or internal resorption
- Vertical root fracture.
- TMJ problems, bruxism, clenching or traumatic occlusion.
- Inability to understand and perform the given instructions.
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, New Cairo, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 40 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, New Cairo, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.