Irreversible Pulpitis Clinical Trial
Official title:
154/2013 Grant for Mineral Trioxide Aggregate and Biodentine for Vital Pulp Therapy
Verified date | September 2019 |
Source | Jordan University of Science and Technology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aimed to evaluate the clinical performance of White MTA (MTA, Angelus, Londrina,
Brazil) and Biodentine™ in pulp capping of cariously exposed mature permanent teeth.
The investigator performed a prospective longitudinal randomized controlled study utilizing
vital permanent mature teeth with deep caries. Patients will be divided randomly into
Biodentine™ and MTA groups; Teeth will be assessed clinically and radiographically prior to
the procedure. Caries will be excavated under local anesthesia, hemostasis is achieved after
pulp exposure using NaOCl and will be capped with Biodentine™ or MTA. Clinical and
radiographical follow-up will be performed by a blinded calibrated evaluator after six months
and one year, and yearly after.
Status | Active, not recruiting |
Enrollment | 60 |
Est. completion date | October 4, 2023 |
Est. primary completion date | December 1, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 16 Years and older |
Eligibility |
Inclusion Criteria: - Teeth that Fulfilled All the Following Criteria Were Selected - Vital teeth responding positively to cold test. - Reversible or irreversible pulpitis with or without periapical lesion. - Deep caries that if removed exposure of the pulp is most likely to occur. - Permanent mature molar, premolar or anterior tooth - The tooth should be restorable. - No serious medical problem that could prevent the patient from receiving the treatment or attending later the follow up visits. Exclusion Criteria: - Exclusion Criteria - Immature tooth - Unrestorable tooth - Tooth that did not respond to cold test - Serious medical problem that could prevent the patient from receiving the treatment or attending later the follow up visits. |
Country | Name | City | State |
---|---|---|---|
Jordan | Dr Lama Awawdeh | Irbid |
Lead Sponsor | Collaborator |
---|---|
Jordan University of Science and Technology |
Jordan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | clinical vital pulp therapy success | Treatment was considered successful based on absence of symptoms and signs | from date of randomization until failure reported for up to 100 months | |
Secondary | Radiographic success | treatment could be further evaluated based on absence of canal oblitration | from date of randomization until failure reported for up to 100 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT04585438 -
Evaluation of Trans-mucosal Bio-adhesive Discs of Diclofenac Potassium on the Anesthetic Success and Postoperative Pain in Patients With Symptomatic Irreversible Pulpitis: A Randomized Clinical Trial
|
Phase 4 | |
Completed |
NCT02923687 -
Premedication Efficacy of Ketorolac Infiltration on Post Endodontic Pain
|
Phase 2 | |
Completed |
NCT02614118 -
Premedication Efficacy of Oral Ketorolac and Ketorolac/ Acetaminophen on Post Treatment Pain
|
Phase 2 | |
Completed |
NCT02601911 -
Effect of Premedication on Success of Inferior Alveolar Nerve Block Injection
|
Phase 2 | |
Completed |
NCT01496846 -
Efficacy Study of Articaine Versus Lidocaine as Supplemental Infiltration in Inflamed Molars
|
Phase 4 | |
Withdrawn |
NCT04040127 -
Residual Dental Pulp Tissue and Cord Blood Stem Cells
|
Phase 2 | |
Completed |
NCT06176378 -
A Clinical and Radiographic Evaluation of Low-Level Diode Laser Full Pulpotomy in Vital Permanent Teeth
|
N/A | |
Recruiting |
NCT04243733 -
MTA vs CEM Pulpotomy in Young Permanent Molars
|
N/A | |
Recruiting |
NCT06245161 -
Efficacy of Computer Controlled Intraosseous Anesthesia in Pediatric Dental Patients
|
N/A | |
Not yet recruiting |
NCT06420583 -
Post Operative Pain and Oral Health Related Quality of Life Following Pulpotomy VS Extraction of Permanent First Molar
|
N/A | |
Not yet recruiting |
NCT04573374 -
Comparing the Outcome of Pulpotomy Using Biodentine and Portland Cement in Mature Cases With Irreversible Pulpitis: Randomized Clinical Trial
|
N/A | |
Completed |
NCT05778227 -
Comparing Different Single and Combination Chelating Agents on Sealer Penetration and Dentin Erosion.
|
N/A | |
Completed |
NCT04654845 -
Patient Perception Between Two Emergency Treatments of Symptomatic Irreversible Pulpitis.
|
N/A | |
Recruiting |
NCT06142799 -
Influence of Moment of Restoration in Pain After a Root Canal Treatment
|
N/A | |
Active, not recruiting |
NCT06240130 -
Outcome Following Use of NaOCl and Chlorhexidine as Wound Lavage Agents
|
N/A | |
Recruiting |
NCT06433245 -
Outcome Following Use of Different Concentrations of NaOCl as Wound Lavage and Hemostatic Agent in Partial Pulpotomy
|
N/A | |
Not yet recruiting |
NCT06427070 -
Effectiveness of Two Intracanal Irrigation Solutions
|
N/A | |
Not yet recruiting |
NCT05349929 -
Analgesic Effect of Anahil and Ibuprofen on Pain After Root Canal Therapy in Patients With Pulpitis of the Molars in Qazvin(a City in Iran)
|
Phase 2 | |
Recruiting |
NCT06149845 -
Pulpotomy in Vital Primary Molars Diagnosed With Symptomatic Irreversible Pulpitis
|
N/A | |
Completed |
NCT01561183 -
Vital Pulp Therapy (VPT) Using Calcium Enriched Mixture (CEM) to Treat Irreversible Pulpitis
|
N/A |