Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
52 participants
INTERVENTIONAL
2017-06-27
2018-07-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Occlusal Reduction and Postoperative Pain
NCT03117062
Occlusal Reduction Effect on Postendodontic Pain
NCT04186897
Comparative Evaluation of the Efficacy of Intraoral Cryotherapy Versus Intracanal Cryotherapy on Postoperative Pain
NCT05041738
Influence of Apical Patency Concept Upon Postoperative Pain After Root Canal Treatment
NCT05170477
Pain After PRP Revascularization and Endodontic Treatment of Non-vital Mandibular Molars With Apical Periodontitis
NCT03350841
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
occlusal surface reduction
occlusal surface reduction after single visit root canal treatment
occlusal surface reduction
occlusal surface reduction after single visit root canal treatment
no occlusal surface reduction
No occlusal surface reduction after single visit root canal treatment
occlusal surface reduction
occlusal surface reduction after single visit root canal treatment
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
occlusal surface reduction
occlusal surface reduction after single visit root canal treatment
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Medically free patients.
3. Patients suffering from symptomatic irreversible pulpitis with symptomatic apical periodontitis in maxillary and mandibular molars with:
* Preoperative pain.
* Vital pulp.
* Sensitivity to percussion.
* Occlusal contact with the opposing teeth.
* Normal periapical radiographic appearance or slight widening in the periodontal membrane space.
Exclusion Criteria
2. Patients having a significant systemic disorder.
3. Patients who had administered analgesics or antibiotics during the last 12 hours preoperatively.
4. Patients having bruxism or clenching.
5. Teeth having :
* No occlusal contact.
* No sensitivity to percussion.
* Association with swelling or fistulous tract.
* Acute or chronic peri-apical abscess.
* Greater than grade I mobility.
* Pocket depth greater than 5mm.
* No possible restorability.
* Previous endodontic treatment
20 Years
50 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cairo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Fadwa sheesh
Bachelor degree of oral and dental medicine
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
evidence comittee
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.