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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03327844
Other study ID # DSRB 2015/00612
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date March 1, 2017
Est. completion date July 31, 2021

Study information

Verified date October 2021
Source National University Health System, Singapore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the efficacy of Antibiotic pastes or Calcium hydroxide disinfection on healing of periapical pathology and continued root development of infected non-vital immature permanent teeth in children. In the test group regenerative endodontic therapy (RET) is performed with antibiotics as the disinfecting agent, in the control group RET is performed with Calcium Hydroxide as the disinfecting agent.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date July 31, 2021
Est. primary completion date July 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 16 Years
Eligibility Inclusion Criteria: 1. Patients aged 6-16 years of age 2. Patients who are fit and healthy or with American Society of Anesthesiologists (ASA) 1 or ASA 2 medical conditions 3. Patients with cooperation level that would allow treatment under local analgesia, application of rubber dam isolation and taking of intraoral radiographs. 4. Patients with permanent premolars that have incomplete root formation with an open apex of greater than 1mm width as observed radiographically and of single root canal morphology (22) 5. Patients with single rooted immature permanent premolars having one of the following pulpal and periapical diagnosis: a. Pulpal i. Necrotic pulp ii. Symptomatic and inflamed pulp not expected to heal. During attempted Cvek or cervical pulpotomy procedures, if the pulpal bleeding does not stop with direct pressure within 5 minutes, pulpectomy will be carried out and the patient will be recruited for RET procedures. b. Periapical i. Symptomatic apical periodontitis (with or without a radiographic apical lesion) ii. Asymptomatic apical periodontitis (with a radiographic apical lesion) iii. Acute apical abscess iv. Chronic apical abscess Teeth will be deemed non-vital if either are non-responsive to sensibility tests (i.e. Electric Pulp test and cold tests), and/or present with signs and symptoms of non-vitality (e.g. swelling and abscess). Exclusion Criteria: 1. Patients aged > 16 years of age. 2. Patient with known allergies to Ciprofloxacin (or any fluoroquinolones class of antibiotics) or metronidazole antibiotics. 3. Patients with medical conditions and/or receiving medications that would affect: 1. Their body's ability to heal e.g. Diabetes; or 2. Their ability to clot efficiently, e.g. Haemophilia 4. Patients with risk of developing infective endocarditis or immune compromised patients. 5. Patients with non-vital permanent premolars where root development is already deemed to be completed (i.e. foramen size of 0-1.0mm diameter as determined radiographically). 6. Impacted or horizontally tilted teeth. 7. Concurrent signs of irreversible pathological root resorption determined radiographically, e.g replacement or internal root resorption, which could otherwise affect the prognosis of the tooth. 8. Uncooperative patients, or those unable to cope with treatment under local anaesthesia, rubber dam isolation and taking of intraoral radiographs.

Study Design


Related Conditions & MeSH terms

  • Infected Immature Permanent Teeth

Intervention

Drug:
RET using antibiotics (Ciprofloxacin and Metronidazole)
RET using antibiotics Ciprofloxacin and Metronidazole. First Treatment Visit: Local analgesic, tooth isolation, access, pulp extirpation and root canal irrigation with 1.5% sodium hypochlorite. Canal drying using paper points. Delivery of mixture of Bi antibiotic paste (Ciprofloxacin and Metronidazole with sterile water). Tooth access sealed with temporary dressing. Second Treatment Visit: Tooth analgesia using plain local analgesics without vasoconstriction, isolation and re-access as described above. Irrigation of root canal system using sodium hypochlorite followed by paper point drying. Initiation of bleeding through insertion of a sterile k-file at a length of 2-3 mm beyond the working length into the periapical tissues. Access sealed using resorbable plug, Biodentine, followed by composite resin.
RET using non-setting Calcium Hydroxide
First Treatment Visit: Local analgesic, Tooth isolation, access, pulp extirpation and root canal irrigation with 1.5% sodium hypochlorite. Canal negotiation, canal drying using paper points. Delivery of the non-setting Calcium Hydroxide. Tooth access sealed with temporary dressing. Second Treatment Visit: Tooth analgesia using plain local analgesics without vasoconstrictor, isolation and re-access as described above. Irrigation of root canal system using sodium hypochlorite followed by paper point drying. Initiation of bleeding through insertion of a sterile k-file at a length of 2-3 mm beyond the working length into the periapical tissues. Access sealed using resorbable plug, Biodentine, followed by composite resin.

Locations

Country Name City State
Singapore National University Hospital Singapore
Singapore School Dental Service, Health Promotion Board Singapore

Sponsors (3)

Lead Sponsor Collaborator
National University Health System, Singapore Health Promotion Board, Singapore, National University, Singapore

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Resolution periapical radiolucency (Clinical evaluation) Clinical evaluation: Presence/Absence of clinical signs of pain and soft tissue pathology (e.g. abscess, sinus tract etc.) 18 months (reviews are at periodicity of 3 months)
Primary Resolution periapical radiolucency (Radiographic evaluation) Size of periapical lesion will be graded using Periapical Index (PAI) 18 months (reviews are at periodicity of 3 months)
Secondary Continued root development (Radiographic evaluation) Quantitative outcomes of lengths and thickness will be measured in millimeters (mm). 18 months (reviews are at periodicity of 3 months)
Secondary Discolouration of tooth Changes in tooth colour will be measured through assessment of photographs 18 months (reviews are at periodicity of 3 months)
Secondary Patient reported outcomes (Perceived oral health-related quality of life (OHRQL)) Oral health related quality of life will be evaluated using the validated questionnaire Child-Oral Impacts on daily performances (C-OIDP) 18 months (reviews are at periodicity of 3 months)
Secondary Patient reported outcomes (Quantitative pain rating) Quantitative pain rating will be done using Faces Pain scale for children 12 years and below; and Numeric Rating scale (NRS) for children 13 years and above.
Faces Pain Scale (range: 0-10); higher scores indicate worse pain
Numeric Rating scale (range: 0-10; 0 - no pain, 1-3 - mild pain, 4-6 - moderate pain, 7-10 - severe pain); higher scores indicate worse pain
18 months (reviews are at periodicity of 3 months)