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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
Postgraduate Institute of Dental Sciences Rohtak
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Apical Periodontitis focused on measuring EDTA, Postoperative pain, Pulp necrosis, Smear layer

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    June 25, 2017
    Last Updated
    September 7, 2017
    Sponsor
    Postgraduate Institute of Dental Sciences Rohtak
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    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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