Periapical Disease Clinical Trial
Official title:
Comparison of the Effects of Different Natural and Synthetic Intracanal Medicaments on the Healing of Periapical Lesion in Retreatment Cases (A Randomized Clinical Trial)
The goal of this clinical trial is to compare the effects of different intracanal medication between endodontic retreatment visits in previously failed root canal treatment patients (single root canal anteriors or premolars teeth). The main question it aims to answer are: - Is natural and synthetic intracanal Medicament effective in reducing or complete healing of Periapical lesions or not? the researchers will compare the effect of different intracanal dressing including: - nanocurcumin gel - curcumin gel - ciprofloxacin +ibuprofen gel - calcium hydroxide Paste as control group in between the endodontic retreatment visits to see if these medicaments work well on periapical lesion healing this outcome measured by Cone beam CT at base and after 1 year follow up period
Status | Not yet recruiting |
Enrollment | 80 |
Est. completion date | November 2025 |
Est. primary completion date | July 20, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility | Inclusion Criteria: - Medically free Patients - both sex includes male and females - Patients age between 20-60 - Patients agreement positively to share in the study - patient able to sign informed consent - on clinical and radiographic examinations, the included teeth maxillary and mandibular single root canal anteriors or premolars suffering from failed endodontic treatment with periapical lesion Exclusion Criteria: - badly broken down teeth indicated for extraction or with difficult isolation - teeth with former procedural errors as ledge, perforation or instrument separation - Medically compromised patients - patients with history of receiving antibiotics within a month before starting study - periodontally affected teeth by pocket depth & > 4mm |
Country | Name | City | State |
---|---|---|---|
Egypt | faculty of dentistry, Ain shams university | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | healing of periapical lesion | measured radiographically the periapical lesion volmetric changes by CBCT between preoperative and after1 year follow up | 1 year | |
Secondary | antibacterial effect (CFU) | Three samples S1 after removal of old root canal filling , S2 after mechanical Preparation , S3 after 7 days of placement of intracanal dressing measuring total bacterial count by colony forming unit each sample cultured and incubated for 24hours and bacterial counting measured | at first visit : S1 :baseline sample, S2 : sample immediately after chemomechanical procedure , at second visit S3: sample after 7 days of placement medication | |
Secondary | Interappointment Pain | measured by Numerical Rating Scale (NRS) which is an 11-point scale consisting of numbers from 0 through 10 0 reading represents "no pain"
1- 3 readings represent "mild pain" 4- 6 readings represent "moderate pain" 7- 10 readings represent "severe pain" No or mild pain was considered as success while moderate or severe pain were regarded as failure. |
6,12, 24, 48, 72 hours after 1st visit |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00490165 -
Periodontal and Periapical Inflammation and Pregnancy
|
N/A | |
Active, not recruiting |
NCT00228280 -
Periapical Bone Healing After Apicectomy With and Without Retrograde Root Filling
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT04358887 -
Effect of Piezoelectric Surgery on Quality of Life and Periradicular Healing After Endodontic Surgery
|
N/A |