Effect of Smear Layer on Endodontic Outcome
Primary Purpose
Apical Periodontitis
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Root canal treatment with smear layer removal
Root canal treatment without smear layer removal
Sponsored by
About this trial
This is an interventional treatment trial for Apical Periodontitis focused on measuring EDTA, Postoperative pain, Pulp necrosis, Smear layer
Eligibility Criteria
Inclusion Criteria:
- Mature permanent mandibular first and second molars requiring primary root canal treatment
- Diagnosis of pulpal necrosis, as confirmed by negative response to cold and electrical tests; and absence of bleeding on entering the pulp chamber
- Radiographic evidence of periapical radiolucency (minimum size ≥ 2.0 × 2.0 mm)
- Patient's age more than 18 years
Exclusion Criteria:
- Patients who do not provide consent for participation in the study
- Age <18 years
- Positive history of antibiotic use within past one month of the treatment
- Patients who are pregnant, diabetic, immunocompromised, had serious medical illness or required antibiotic premedication
- Patients with pockets ≥4mm or having marginal or furcal bone loss due to periodontitis
- Teeth that are not suitable for rubber dam isolation
- Previously accessed teeth and/or with procedural errors
- Unrestorable tooth, fractured/ perforated roots, inflammatory root resorption
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Smear Layer Positive
Smear layer negative
Arm Description
Root canal treatment without smear layer removal: Root canal treatment and Irrigation with 1 ml of 2.5% sodium' hypochlorite for 1 min, followed by ultrasonic activation of 3 ml of 2.5% sodium hypochlorite for 1minute.
root canal treatment with smear layer removal:Root canal treatment and Irrigation with 1 mL of 17% EDTA solution and ultrasonic activation, followed by ultrasonic activation of 3 ml of 2.5% sodium hypochlorite for 1 minute.
Outcomes
Primary Outcome Measures
Radiographic success
Size of apical radiolucency were scored according to PAI scores and PAI score less than 3 were considered as success
Clinical success
Presence or absence of any clinical symptoms such as pain,tenderness, sinus tract and swelling
Secondary Outcome Measures
Pain intensity
Pain intensity before and after treatment. Intensity of pain was recorded using 10 cm VAS scale with 0 depicting no pain and 10 depicting maximum pain imaginable.
Full Information
NCT ID
NCT03277404
First Posted
June 25, 2017
Last Updated
September 7, 2017
Sponsor
Postgraduate Institute of Dental Sciences Rohtak
1. Study Identification
Unique Protocol Identification Number
NCT03277404
Brief Title
Effect of Smear Layer on Endodontic Outcome
Official Title
Effect of Smear Layer on Endodontic Outcome: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
May 7, 2015 (Actual)
Primary Completion Date
November 30, 2015 (Actual)
Study Completion Date
November 30, 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Postgraduate Institute of Dental Sciences Rohtak
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluated the effect of removal of smear layer on the success of primary root canal treatment.Patients requiring primary root canal treatment in mature mandibular first and second molars were allocated to either smear layer positive group and smear layer negative group.
Detailed Description
Patients requiring primary root canal treatment following the diagnosis of pulp necrosis in permanent mandibular first and second molars having radiographic evidence of periapical radiolucency (minimum size ≥ 2.0 × 2.0 mm) were included in the study. All patients were over 18 years of age and diagnosis of pulpal necrosis was confirmed by negative response to cold and electrical tests, and absence of bleeding on entering the pulp chamber. Patients with systemic illness, history of analgesic intake within past 7 days, antibiotics in the last 3months and patients who were pregnant were excluded from the study. Periodontally compromised teeth, previously accessed teeth, teeth that were not suitable for rubber dam isolation were also excluded from the study.
Subjects were allocated to one of the two study groups: smear layer positive group (only 2.5%NaOCl was used) - SP and smear layer negative group (17% EDTA+2.5%NaOCl was used) - SN. Using an equal proportion randomization allocation ratio, patients were assigned to the two groups using envelopes containing concealed assignment codes. It was ensured that neither the patient, nor the primary investigator was aware of the group till the time of final rinse.
After administration of local anesthesia, rubber dam isolation of the involved tooth was done. Caries was excavated and access cavity prepared using carbide burs in high speed handpiece with copious irrigation.Debridement of the pulp chamber was done and all canal orifices identified.Working length was obtained with the help of electronic apex locator and confirmed radiographically.Hand files number 10, 15 and 20 were used till working length (WL) to prepare a smooth reproducible glide path.Canal preparation was done with the help of rotary NiTi files. In both groups, 2.5% sodium hypochlorite was used as irrigant after each instrument. All the irrigation procedures were performed using a 27 gauge side vented needle. After root canal instrumentation, 17% Ethylenediaminetetraacetic acid (EDTA) solution was also used to remove smear layer in smear layer negative group, while teeth in smear layer positive group was simply rinsed with 2.5% sodium hypochlorite. In both the groups ultrasonic activation of irrigant was done. An inter-appointment dressing of calcium hydroxide was given. The access cavity was then restored with intermediate restorative material (Dental Products of India).
Patients were prescribed Ibuprofen 400mg with the instructions to take one tablet every 8 hours in the event of pain.Patients were asked to record the severity of pain using 10 cm VAS scale with 0 depicting no pain and 10 depicting maximum pain imaginable. Patients were asked to make a mark on the line that represented their level of perceived pain every 24hrs for 7 days following intervention.
One week later, patients returned with the completed questionnaires.
At the same appointment the intracanal dressing was removed with H-files and copious irrigation with 2.5% NaOCl in both the groups.
17% EDTA solution was used to remove smear layer in smear layer negative group, followed by 2.5% NaOCl while teeth in smear layer positive group were simply rinsed with 2.5% sodium hypochlorite.
Ultrasonic activation of irrigant was done and canals were obturated with the GuttaPercha and Zinc Oxide-Eugenol based sealer in both the groups. After obturation, the cavity was restored permanently.Immediate post-operative radiograph was then taken using preset exposure parameters.Follow up clinical and radiographic examination was carried out every 3 months, till a 12 month period. The data gathered was analyzed using suitable statistical methods.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Apical Periodontitis
Keywords
EDTA, Postoperative pain, Pulp necrosis, Smear layer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
86 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Smear Layer Positive
Arm Type
Experimental
Arm Description
Root canal treatment without smear layer removal: Root canal treatment and Irrigation with 1 ml of 2.5% sodium' hypochlorite for 1 min, followed by ultrasonic activation of 3 ml of 2.5% sodium hypochlorite for 1minute.
Arm Title
Smear layer negative
Arm Type
Active Comparator
Arm Description
root canal treatment with smear layer removal:Root canal treatment and Irrigation with 1 mL of 17% EDTA solution and ultrasonic activation, followed by ultrasonic activation of 3 ml of 2.5% sodium hypochlorite for 1 minute.
Intervention Type
Procedure
Intervention Name(s)
Root canal treatment with smear layer removal
Other Intervention Name(s)
irrigation with EDTA
Intervention Description
Canal were irrigated with Naocl and EDTA to remove smear layer
Intervention Type
Procedure
Intervention Name(s)
Root canal treatment without smear layer removal
Other Intervention Name(s)
irrigation with only NAOCL
Intervention Description
only sodium hypochlorite was used for irrigation
Primary Outcome Measure Information:
Title
Radiographic success
Description
Size of apical radiolucency were scored according to PAI scores and PAI score less than 3 were considered as success
Time Frame
every 3 months till 12 month period
Title
Clinical success
Description
Presence or absence of any clinical symptoms such as pain,tenderness, sinus tract and swelling
Time Frame
till 12 months
Secondary Outcome Measure Information:
Title
Pain intensity
Description
Pain intensity before and after treatment. Intensity of pain was recorded using 10 cm VAS scale with 0 depicting no pain and 10 depicting maximum pain imaginable.
Time Frame
Patients were asked to make a mark on the line that represented their level of perceived pain every 24hrs for7 days following intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mature permanent mandibular first and second molars requiring primary root canal treatment
Diagnosis of pulpal necrosis, as confirmed by negative response to cold and electrical tests; and absence of bleeding on entering the pulp chamber
Radiographic evidence of periapical radiolucency (minimum size ≥ 2.0 × 2.0 mm)
Patient's age more than 18 years
Exclusion Criteria:
Patients who do not provide consent for participation in the study
Age <18 years
Positive history of antibiotic use within past one month of the treatment
Patients who are pregnant, diabetic, immunocompromised, had serious medical illness or required antibiotic premedication
Patients with pockets ≥4mm or having marginal or furcal bone loss due to periodontitis
Teeth that are not suitable for rubber dam isolation
Previously accessed teeth and/or with procedural errors
Unrestorable tooth, fractured/ perforated roots, inflammatory root resorption
12. IPD Sharing Statement
Plan to Share IPD
No
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Effect of Smear Layer on Endodontic Outcome
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