Actively Recruiting
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
Led by Future University in Egypt · Updated on 2024-10-15
30
Participants Needed
1
Research Sites
73 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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. Understanding these factors helps professionals select methods and supplies to minimize discomfort. 30 patients will be divided into 3 groups according to the method of activation (10 par ticipants/each). participants will be recruited from the postgrad clinic of the endodontic department faculty of oral and dental medicine, Future University in Egypt Patients with mature mandibular first permanent molar with irreversible pulpitis with apical periodontitis Intervention 1: bio-ceramic sealer activation with Eddy sonic Intervention 2: bio-ceramic sealer activation with AF max Control/Comparator: bio-ceramic sealer without activation The study aims to evaluate the effect of Eddy Sonic and AF max activation of bio-ceramic sealer on postoperative pain in mandibular first molars with symptomatic irreversible pulpitis with apical periodontitis
CONDITIONS
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
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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.
- Systemically healthy patient (ASA I, II).
- 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.
You will not qualify if you...
- Patients with American Association of Anesthesiologists (ASA) classifications other than ASA I or II.
- Patients who have taken preoperative medication such as analgesics, non-steroidal, or steroidal anti-inflammatory drugs within 12 hours before treatment.
- Patients with NSAID allergy.
- Patients having two or more adjacent teeth needing root canal therapy.
- Pregnant patients.
- Patients with bleeding disorders.
- Patients with long-term corticosteroid use.
- Teeth with necrotic pulp.
- History or presence of swelling or fistulous tract.
- Acute or chronic periapical abscess.
- Tooth mobility more than grade 1.
- Periodontal pocket depth more than 5 mm.
- Teeth not restorable.
- Previous root canal treatment.
- Presence of periapical radiolucency.
- External or internal root resorption.
- Vertical root fracture.
- Temporomandibular joint problems, bruxism, clenching, or traumatic occlusion.
- Inability to understand and perform the given instructions.
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Trial Site Locations
Total: 1 location
1
Future University in Egypt
Cairo, New Cairo, Egypt, 11835
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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