- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06643676
Effect of Targeted Endodontic Microsurgery on Quality of Life and Healing on Mandibular Molars
Effect of Targeted Endodontic Microsurgery on Quality of Life and Healing on Mandibular Molars : A Randomized Controlled Trial
Study Overview
Status
Conditions
Detailed Description
Conventional Endodontic microsurgery takes use of a preoperative scan and manual drilling of the osteotomy site with arbitrary measurements followed by retropreparation and forming the apical seal. One of the most critical disadvantages of conventional root-end resection include the damage to anatomically vital structures such as inferior dental nerve, mental nerve, adjacent root and maxillary sinus. In contrast, endodontic microsurgery using the guide template significantly reduces these damages. Pinsky et al confirmed in their in vitro study that the greater accuracyand consistency was achieved during endodontic surgery with surgical guidance without damaging vital structures. An error greater than 3 mm occurred over 22% of the time with freehand whereas none of errors occurred with surgical guidance.
Consequently, targeted endodontic microsurgery has garnered increasing attention as a viable alternative, offering a refined and precise approach to address such challenges.
Even the most skilled surgeons may find endodontic microsurgery difficult. Some medical professionals steer clear using freehand (FH) Endodontic microsurgery in regions where there is a chance of harming important anatomical features including the maxillary sinus, the mental foramen, and arteries. It is Perceived as complex sites include those with limited access, no direct sight, and areas where the apex is placed distant from the buccal cortical bone without any cortical plate fenestratio. Surgeons may be able to perform precise procedures in difficult-to-reach regions with guided Endodontic Microsurgery
Guided Endodontic Microsurgery is virtually planned on 3D software on the preoperative CBCT scan, and the surgeon executes the osteotomy and root-end resection (RER) under static or dynamic navigation.
Static navigation requires a customized 3D-printed surgical guide (3D-SG) to guide the drilling duringosteotomy and RER. Surgical guides contain a guide template that refers to the 3D location of the virtual Endodontic Microsurgery planned in the CBCT to drill accurately Prior research has demonstrated that 3D-SG can reduce the risk of intra-operative complications whileincreasing the precision and effectiveness of EMS. In comparison to free hand Endodontic Microsurgery, guided Endodontic Microsurgery with 3D-Surgical Guide shortens the surgical time, provides superior control over the resection level and bevel off the root, and enables a tailored osteotomy size.
Trephine burs have been used for the removal of failed implants and autogenous bone graft harvesting but have not previously been described in Endodontic Microsurgery .
Targeted Endodontic Microsurgery produces a single-step osteotomy; root-end resection; and biopsy with a defined perforation site, angulation, depth, and diameter. Previous reports have used 3D Surgical Guides to locate an ideal bone perforation site, but none have used trephine burs within a stent to define all parameters of osteotomy and root-end resection.
Also, no clinical study assessing the targeted approach of endodontic microsurgery with Oral health related quality of life has been done. Some of the RCT's are conducted assessing quality of life in patients after conventional periapical surgery, only two retrospective studies considering .Targeted Endodontic Microsurgery have been done and a lack of RCTs comparing targeted Endodontic Microsurgery with conventionalEMS warrants further research.
The aim of this study is to compare the effect of a static computer-aided surgical technique using a 3D- printed guide with a fully guided drill protocol on Oral Health Related Quality of Life against the conventional endodontic microsurgery in mandibular molars.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Haryana
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Rohtak, Haryana, India, 124001
- Post Graduate Institute of Dental Sciences , Rohtak
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients in which non-surgical retreatment is unfeasible (post, anatomical complexity, iatrogenic errors) or previously failed treatment.
- Patients with persistent symptomatic apical periodontitis and periapical radiolucency.
- Tooth with a peri-radicular lesion of strictly endodontic origin (chronic apical periodontitis) and combined endodontic periodontic lesions with the size of lesion ≥5mm.
Patients between 18-55 years of age.
- No general medical contraindications for oral surgical procedures (ASA-1 and ASA-2 according to the classification of the American Society of Anesthesiologists)
- ASA 1- A normal healthy patient. Example: Fit, nonobese (BMI under 30), nonsmoking patient with good exercise tolerance.
- Tooth with adequate final restoration without clinical evidence of coronal leakage.
- No spontaneous pain or swelling.
- Good periodontal health condition at tooth level
- Able to completely understand and sign an informed consent form
Exclusion Criteria:
- Patients with systemic diseases (diabetes mellitus, uncontrolled hypertension grade III, hepatic/renal disease, or systemic bleeding disorders)
- Patients on anticoagulant/ antiplatelet drugs.
- Fractured/perforated teeth.
- Teeth with deep pockets (probing depth > 4 mm).
- Presence of vertical root fracture.
- Miller class III/IV mobility.
- Pregnancy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Targeted Endodontic Microsurgery using trephine drill and 3d printed surgical guide
Endodontic Microsurgery using 3d printed static surgical guide using patient's cbct data
|
Patients with apical periodontitis with intact cortex in madibular molars receiving Targeted Endodontic surgery or Guided Endodontic Microsurgery with surgical guide fabricated using the cbct data following failure of non surgical root canal treatment
Other Names:
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|
Active Comparator: Conventional Endodontic microsurgery using burs
Conventional Endodontic microsurgery using carbide bur and free hand conventional procedure
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A conventional endodontic microsurgery using arbitrary localisation technique using the cbct data and performing the surgery with a carbide bur.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life following periapical surgery
Time Frame: 1 year
|
Quality of life quantified using Questionnaire to both groups
|
1 year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Radiographic healing
Time Frame: 1 year
|
two dimensional radiographic healing by rud and molten criteria three dimensional radiographic healing with Cbct by modified Penn criteria
|
1 year
|
|
Time Taken for surgery(Till osteotomy and root end resection)
Time Frame: one year
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Time taken to complete surgery in both the groups
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one year
|
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Accuracy of surgical access
Time Frame: one year
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Osteotomy size was assessed intraoperatively in both the TEMS and CEMS groupsimmediately after completion of the osteotomy and root-end resection.
The maximum mesiodistal width and apicocoronal height of the osteotomy were measured at the level of the buccal cortical plate using a periodonal probe, which served as the standardized anatomical reference for both surgical techniques.
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one year
|
Collaborators and Investigators
Investigators
- Study Director: Jigyasa grover, MDS, PGIDS ROHTAK, HARYANA
- Study Chair: sanjay Tewari, MDS, PGIDS ROHTAK HARYANA
- Principal Investigator: MOHAMMED MUZAFFAR KHAN, BDS, PGIDS ROHTAK HARYANA
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Musculoskeletal Diseases
- Periodontal Diseases
- Mouth Diseases
- Stomatognathic Diseases
- Neoplasms
- Jaw Diseases
- Cysts
- Odontogenic Cysts
- Jaw Cysts
- Bone Cysts
- Periodontitis
- Periodontal Cyst
- Periapical Periodontitis
- Periapical Diseases
- Radicular Cyst
- Periapical Granuloma
- Surgical Procedures, Operative
- Dentistry
- Oral Surgical Procedures
- Endodontics
- Apicoectomy
Other Study ID Numbers
- Muzaffar Khan
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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