Endodontic Disease

14

Review clinical trials related to Endodontic Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Exploration of the Utility of Dental-dedicated MRI for Dentistry

This description observational research is comparative in design, that is comparing existing standard clinical dental images, not obtained in this study, to test (i.e., ddMRI) images. The standard clinical dental images consist of radiographs, such as bitewings, periapical, panoramic, cone-beam CT, and medical CT, as well medical MRIs of the temporomandibular joints (TMJ).The conceptualization of research questions, study designing, and interpretation of imaging data has and will involve content expertise in all ddMRI research.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of MinnesotaUpdated: May 20, 2026Locations: 1
Eligibility criteria

Patient Age: 18 years old or older [+6]

Unable to consent to participant in English [+4]

Status: Not yet recruiting

Nanozymes in Endodontics

The antimicrobial efficacy and healing potential of clinically approved ferumoxytol nanozymes versus the standard 3% NaOCl irrigant will be evaluated in adults undergoing endodontic treatment. Building on prior protocols that demonstrated ferumoxytol nanozymes antimicrobial activity as a root canal irrigant, ferumoxytol solution will be applied topically, assessment of clinical and radiographical findings will determine its potential as a novel disinfection and its long-term outcome.

Participants needed: 72
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of PennsylvaniaUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Patients willing to participate in the study. [+8]

Self-reported pregnancy. [+8]

Status: Recruiting

A Randomized Controlled Trial Evaluating Whether Pre-operative Trinase Reduces Post-operative Pain in Patients With Symptomatic Irreversible Pulpitis Compared to Placebo, Using VAS Scores and Analgesic Intake Over 48 Hours.

This study aims to determine whether Trinase, an enzyme-based anti-inflammatory medication, can reduce pain after root canal treatment in patients with symptomatic irreversible pulpitis. A total of 182 male patients aged 18 to 50 years who present with moderate to severe tooth pain will be randomly assigned to receive either a Trinase tablet or a placebo 30 minutes before treatment. All root canal procedures will be performed in a single visit using standard endodontic techniques. Pain levels will be measured on a Visual Analogue Scale (VAS) before treatment and at 6, 12, 24, and 48 hours after treatment. Patients will also record the number of pain-relief tablets they take during the first 48 hours. The goal of the study is to see whether Trinase can lower post-operative pain and reduce the need for analgesic medication compared with placebo. This information may help improve pain management for patients undergoing root canal therapy.

Participants needed: 182
Trial details
Age: 18-50Biological sex: MaleType: InterventionalSponsor: Fayoum UniversityUpdated: Dec 1, 2025Locations: 1
Eligibility criteria

Systemically healthy male patients (ASA I or II) [+4]

History of allergy or intolerance to Trinase or any of its components (trypsin,... [+6]

Status: Recruiting

The Antimicrobial Potential of Diclofenac Sodium as an Intracanal Medicament

The goal of this randomized clinical trial is to evaluate the capability of the material to exert bacterial reduction of diclofenac sodium versus of that calcium hydroxide paste when these materials are used as intracanal medications in permanent molar teeth with chronic apical periodontitis. The main question\[s\] it aims to answer are: • Will the diclofenac sodium (NSAIDs) possess antimicrobial efficacy to be used effectively as an intracanal medicament similar to that of calcium hydroxide in primary endodontic treatment? Participants will be allocated randomly into three equal groups by using computer generated randomization, according to the type of intracanal medication.

Participants needed: 48
Trial details
Phase: Phase 2, Phase 3Age: 18-50Biological sex: AllType: InterventionalSponsor: British University In EgyptUpdated: May 30, 2025Locations: 1
Eligibility criteria

Patients with teeth diagnosed with apical periodontitis [+2]

Teeth with immature roots [+4]

Status: Recruiting

Effect of Photobiomodulation to Reduce Post-operative Pain After Endodontic Surgery

The objective of this study will be to evaluate if photobiomodulation (FBM) can reduce postoperative pain in patients who will undergo endodontic surgery. For this randomized, controlled and double-blind clinical study, 34 patients without comorbidities who need endodontic surgery in the upper jaw (15 to 25 teeth) will be recruited. They will be randomly divided into an experimental group (n = 17) photobiomodulation (808nm, 100 mW, and 4J/cm2 with 5 points per vestibular). Applications will be made in the immediate postoperative period and 24 hours after surgery. Control group (n = 17) a FBM simulation will be performed in the same way as in the experimental group. In this group, the required analgesia will be administered within the standard with ibuprofen. Both groups will perform the necessary conventional procedures considered the gold standard in the literature. Both the patient and the evaluator will be blinded to the intervention performed. The primary outcome variable of the study will be postoperative pain, which will be assessed using the visual analog scale at all postoperative control visits (baseline, 24 hours and 7 days). As for the secondary outcome variables, the amount of systemic medication received according to the patient's need (will be provided by the investigator).. Radiographic images will be obtained after 1 and 2 months for evaluation of the repair (dimensions of the lesion, radiopacity). These radiographs will be taken digitally with the positioners implemented. Edema, ecchymosis, and evaluation of soft tissues in the anterior portion of the intra and extra-oral maxilla will also be evaluated. In addition, a digital thermometer. These parameters will be evaluated 24 hours and 7 days after the intervention. The X-rays will be taken in the 1st and 3rd month respectively.

Participants needed: 34
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University of Nove de JulhoUpdated: May 7, 2025Locations: 1
Eligibility criteria

Patients with not comorbidities, [+3]

Who are taking drugs that affect bone metabolism and the inflammatory process (f... [+4]

Status: Not yet recruiting

Postoperative Pain and Incidence of Extrusion Following the Use of Two Intra-canal Medications in Retreatment of Single Rooted Teeth

This study aims to compare the postoperative pain and incidence of extrusion of two intracanal medications in the retreatment of single-rooted teeth. The main question it aims to answer is: Does the injection of intra-canal medication into the shaped root canal after complete removal of the old obturating material lead to post-operative pain and paste extrusion to periapical tissues or not?

Participants needed: 30
Trial details
Phase: Phase 2Age: 16-40Biological sex: AllType: InterventionalSponsor: Minia UniversityUpdated: Apr 6, 2025
Eligibility criteria

Patients with failed endodontic treatment in single root teeth [+1]

Muktirooted teeth

Status: Recruiting

Role of GTR on Healing Outcome & Quality of Life in Combined Endo Perio Lesions With Communication

The recovery of periapical defects linked to periodontal communication frequently yields less satisfactory results. Numerous studies and case reports have highlighted the notable success achieved through the application of guided tissue regeneration techniques. More recently, autologous platelet concentrate plug \& placental membrane have emerged as a treatment option for addressing such lesions. Nevertheless, there has been no study using PRF-Medium with ACM membrane on the healing of aforesaid lesion \& quality of life assessment.

Participants needed: 30
Trial details
Age: 16+Biological sex: AllType: InterventionalSponsor: Postgraduate Institute of Dental Sciences RohtakUpdated: Jan 8, 2025Locations: 1
Eligibility criteria

Patients of age 16yrs and above. [+5]

Presence of vertical root fracture [+5]

Status: Recruiting

Irrigation Activating Techniques on Irrigant Penetration Depth and Microbial Reduction

This in-vivo study aim to evaluate effect of different irrigation activating techniques on Irrigant Penetration Depth and Microbial Reduction in root Canals

Participants needed: 30
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Oct 28, 2024Locations: 1
Eligibility criteria

• Asymptomatic vital/non vital teeth requiring root canal treatment. [+4]

• Patients with any systemic diseases. [+4]

Status: Recruiting

Effect of Photobiomodulation on Pain and Healing of the Vertical Releasing Incision After Endodontic Microsurgery

The purpose of this study is to evaluate the effect of Photobiomodulation (PBM) in postoperative pain after endodontic microsurgery (EMS) in patients from the University of Texas Health Science Center at Houston, School of Dentistry Graduate Endodontic Clinic and to assess the soft tissue healing of the vertical releasing incision (VRI) after PBM

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Aug 29, 2024Locations: 1
Eligibility criteria

American Society of Anesthesiologists (ASA) I or II. [+2]

ASA III or IV. [+8]

Status: Recruiting

Anti-bacterial Potential of Nano Calcium Hydroxide as an Intracanal Medication

The aim of the study is to evaluate the anti-bacterial potential of Nano Calcium Hydroxide as an intracanal medication in primary endodontic treatment of permanent molars.

Participants needed: 54
Trial details
Phase: Phase 2, Phase 3Age: 21-49Biological sex: AllType: InterventionalSponsor: British University In EgyptUpdated: Aug 19, 2024Locations: 1
Eligibility criteria

healthy males and females. [+3]

pregnant women. [+5]

Status: Recruiting

Antimicrobial Efficacy of Nano-Based ICM on E.F

This in-vivo study aims to evaluate the antimicrobial effect of nano based intracanal medications (Triple antibiotic-loaded chitosan nanoparticles and chlorohexidine loaded by silver nanoparticles) on Enterococcus faecalis count reduction in secondary endodontic infection cases.

Participants needed: 30
Trial details
Age: 19-60Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Aug 1, 2024Locations: 1
Eligibility criteria

Single rooted, single canal premolar teeth. [+5]

Patients with any systemic diseases. [+7]

Status: Not yet recruiting

Endo-perio Disease - Treatment Outcomes Using Conventional and Hydraulic Calcium Silicate Sealer With or Without LPRF

The endodontic periodontal-disease is characterized by the involvement of the pulp and periodontal disease in the same tooth. The anatomic connections between the dental pulp and the periodontium provide a pathway for perio-endo communication via apical foramina, lateral canals, exposed dentinal tubules, and developmental grooves. These pathways provide an egress for pulpal disease to affect the periodontium and conversely, an ingress for periodontal disease to affect the pulp. Teeth with endo-perio disease, which are deemed salvageable might require root canal (endodontic) treatment, followed by staged periodontal treatment. Compared to conventional sealers used for endodontic treatment, the hydraulic calcium silicate based sealers (HCSB)s have excellent sealing ability, biocompatibility, regeneration ability, and antimicrobial characteristics. However little is known about its clinical benefits when used to treat endo-perio disease. The gold standard treatment for periodontitis affected teeth associated with intrabony lesions is guided tissue regeneration (GTR) which has significant improved clinical outcomes over open flap debridement (Cochrane systematic review 2005). However, the success the of this regenerative technique requires careful case and defect selection. We propose the use of an autologous bioactive scaffold, leukocyte platelet rich fibrin (L-PRF) to achieve regeneration of periodontal soft and hard tissues, resulting in faster healing, greater bone infill and improved predictability of clinical outcomes

Participants needed: 115
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: King's College LondonUpdated: Jan 12, 2023Locations: 1
Eligibility criteria

• Diagnosis of Endodontic-periodontal disease without root damage in periodontit... [+3]

Endodontic considerations: severely sclerosed canals, external cervical resorpti... [+14]

Status: Recruiting

Outcome of Endodontic Treatment and Retreatment With a Bioceramic Sealer

This study is a prospective randomized controlled study of patients who come to the University. The aim is to evaluate the success rate of treatment and retreatment of canals using BioRoot ™ RCS cement compared with AH Plus up to 6 years of follow-up. The null hypothesis is that there will be no statistically significant differences in rates of successful treatment of root canals filled with BioRoot ™ RCS compared to gutta-percha and AH Plus sealer.

Participants needed: 220
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Juan Gonzalo OlivieriUpdated: Aug 31, 2020Locations: 1
Eligibility criteria

Patients that demonstrate understanding of the study and willingness to particip... [+5]

General: Patients with systemic diseases, diabetes, immunocompromised and pregna... [+1]

Status: Recruiting

Outcome of Endodontic Retreatment in One or Two Visits

This study is a prospective randomized controlled study of patients who come to the University and non-surgical root canal retreatment is considered as the election of choice in presence of periapical disease. The aim is to evaluate the success rate of non-surgical retreatment performed in one compared to two visit treatment up to 10 years of follow-up. The null hypothesis is that there will be no statistically significant differences in rates of success, when performing root canal non-surgical retreatment in one or two visits.

Participants needed: 110
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Universitat Internacional de CatalunyaUpdated: Aug 26, 2020Locations: 1
Eligibility criteria

Patients that demonstrate understanding of the study and willingness to particip... [+5]

General: Patients with systemic diseases, diabetes, immunocompromised and pregna... [+1]