Periodontal and Endodontic Lesion Clinical Trial
Official title:
Surgical Periodontal Intervention With Simultaneous Versus Delayed Endodontic Treatment in Concurrent Endodontic-Periodontal Lesion Without Communication - An Interventional Study
The aim of this study is to evaluate the periodontal parameters in terms of periodontal healing by periodontal surgical therapy with simultaneous or delayed endodontic therapy in management of concurrent endodontic -periodontal lesion without communication
INTRODUCTION
The term " Endodontic-Periodontal " lesion has been proposed to describe the destructive
lesions resulting from inflammatory products found in varying degrees in both the
periodontium and the pulpal tissues. The term concurrent endodontic periodontal lesion
without communication applies to a tooth that has an infected root canal system with some
form of apical periodontitis plus marginal periodontal disease with pocketing but the
periapical and periodontal disease do not communicate with each other.
Although there are many factors, the primary cause of both diseases is the presence of
bacterial infection with complex microbial flora. Based on microbiological studies many
authors have reported the similarity between bacterial flora associated with endodontic and
periodontal infections. Therefore periodontal pocket may be a source of bacteria for root
canal system or vice versa and cross seeding of bacteria can occur in either direction
through communication pathways. An untreated infection of one of these tissues can lead to
signs or symptoms of disease within the other tissue.
Observations based upon review articles and case reports has suggested, if the root canal
system is infected, endodontic treatment should be commenced prior to any periodontal therapy
in order to remove the intra-canal infection before any cementum is removed in case of
concurrent endodontic - periodontal lesions without communication. Treatment results of
endodontic therapy should be evaluated in 2-3 months and only then periodontal treatment
should be considered.
Concerns about the possibility that endodontically treated teeth might not respond to
periodontal therapy are certainly not new. Histological examination of human teeth concluded
that endodontic therapy had adversely affected periodontal healing. Teeth that had undergone
endodontic therapy did not respond well to regenerative procedures as teeth that had not
undergone such treatment. It has been advocated to perform periodontal therapy before
endodontic obturation because of the concern that the leakage of endodontic sealer would
hinder repair, regeneration or both. There is a negative impact of certain root canal filling
materials on fibroblast attachment to the dentin surface of extracted third molars. Also
endodontic therapy performed simultaneously with or soon after periodontal surgery adversely
affected the formation of new bone, new cementum and new attachment. It was also found in a
study that periapical pathology was not significantly correlated to mean pocket depth
reduction after non surgical and surgical treatment of horizontal and vertical defects .
The microflora in infected root canals of teeth that have concurrent endodontic and
periodontal diseases is more complex than in teeth with infection confined to the periapical
region.
All the above findings are based on microbiological, histological, case-reports,
retrospective and in vitro studies, management of concurrent endodontic periodontal lesions
need more evidence based investigations. So far no clinical study has compared periodontal
healing along with or without endodontic therapy. It is hypothesized that endodontic
treatment did not influence the periodontal outcomes after periodontal surgery in
endodontic-periodontal lesion without communication.
Thus the aim of our study is to evaluate the periodontal parameters in terms of periodontal
healing by periodontal surgical therapy with simultaneous or delayed endodontic therapy in
management of concurrent endodontic -periodontal lesion without communication.
MATERIAL AND METHOD
This study will be conducted in Department of Periodontics and Oral Implantology in
collaboration with Department of Conservative Dentistry and Endodontics, Post Graduate
Institute of Dental Sciences , Rohtak.
STUDY POPULATION Patients will be recruited from regular out patient department of the
Department of Periodontics and Oral Implantology, Department of Conservative Dentistry &
Endodontics and Department of Oral medicine, Diagnosis and Radiology.The study will be
conducted as follows:- This Interventional study will include systemically healthy minimum 36
patients with chronic periodontitis having at least one tooth involving endodontic
periodontal lesion which will be further divided into two groups (minimum 18 each) based on
patient's consent for treatment.
1. Simultaneous endodontic periodontal therapy group (Group 1) Scaling and root planning
will be performed simultaneously with non surgical endodontic treatment (in the form of
root canal treatment). After 6 weeks of scaling and root planning , periodontal surgery
will be performed in the form of open flap debridement.
2. Delayed endodontic therapy group (Group 2) Periodontal treatment initiated with scaling
and root planning followed by periodontal surgery in the form of open flap debridement
after 6 weeks. Endodontic treatment will be initiated after 3 months of periodontal
surgery.
Prior informed consent will be taken from each patient after explaining the procedure in
patient's language along with risk and benefits involved.
METHODOLOGY Patients will be allocated to group1 and group 2. The study will be conducted as
follows:- Presurgical therapy:- which will be including
i. Oral hygiene instructions ii. Full mouth supragingival and subgingival scaling and root
planning with ultrasonic scaler, hand scaler and curettes.
iii. In group 1 conventional root canal therapy will be performed simultaneously to
presurgical therapy.
Surgical therapy:- In both groups periodontal surgical procedure in the form of open flap
debridement will be performed after 6 weeks of SRP.
A probing stent will be fabricated for every patient,relative to which attachment loss will
be measured.
In group 2 conventional root canal therapy will be performed 3 months after periodontal
surgical procedure.
CLINICAL PARAMETERS
1. Full mouth indices to be recorded at baseline
- Bleeding on probing
- Probing Pocket depth
- Attachment loss
2. Site specific indices
- Plaque index
- Gingival index
- Probing Pocket depth
- Relative attachment loss
- Bleeding on probing
- Tooth mobility
- Relative gingival marginal level Using UNC 15 periodontal probe at 6 sites (mesial,
distal, median points at buccal and lingual aspects) per tooth.
Customized bite blocks and parallel angle technique will be used to obtain radiographs.
Clinical parameters will be recorded at baseline, at 6 weeks of nonsurgical phase, at 3
months and after 6 months post surgery for Group 1(6 months of periodontal surgery and
endodontic treatment) and group 2 (6 months of periodontal surgery and 3 months of root canal
treatment).
PERIODONTAL NON SURGICAL PROCEDURE This involves supragingival and subgingival scaling and
root planning to be performed with ultrasonic scaler, hand scaler and curette and will be
completed in minimum two sessions.
PERIODONTAL SURGICAL PROCEDURE After administration of local anaesthesia, buccal and
lingual/palatal intracrevicular incision will be made and mucoperiosteal flaps will be
reflected including atleast one tooth ahead and another behind the tooth. Meticulous defect
debridement and root planning will be carried out using area specific curettes and scalers
with special effort to remove all the granulation tissue. After instrumentation, the root
surfaces will be washed with saline solution in attempt to remove any remaining detached
fragments from the defect and surgical field. After debridement mucoperiosteal flaps will be
repositioned and secured by using 3-0 non absorbable black silk surgical suture. The surgical
area will be protected and covered with periodontal dressing and post operative instructions
will be given.
-Instructions will be given for gentle brushing with soft brush and reinstructed for proper
oral hygiene postoperatively and will be examined weekly for up to 1 month after surgery and
again at 3 month.
CONVENTIONAL ENDODONTIC PROCEDURE After achieving local anaesthesia, access opening will be
made with the help of round bur. Then the root canal will be thoroughly debrided followed by
copious irrigation and subsequently prepared with the help of endo files. After preparation
of the canal, calcium hydroxide intracanal medicament will be placed with the help of 27
gauge endodontic syringe for 10 days and access cavity will be sealed with suitable sealer.
Obturation will be performed with gutta percha and zinc oxide eugenol based sealer.
-All parameters will be re-evaluated at recall period of 6 weeks, 3 months and 6 months for
Group 1 (conventional endodontic periodontal therapy group) and group 2 (delayed endodontic
therapy group).
STATISTICAL ANALYSIS
Data recorded will be processed by standard statistical analysis.
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Status | Clinical Trial | Phase | |
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Active, not recruiting |
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