search
Back to results

Effect of Bromelain Versus Calcium Hydroxide as an Intracanal Medication on the Intensity of Postoperative Pain and Bacterial Load Reduction in Necrotic Single Rooted Lower Premolars

Primary Purpose

Intracanal Medication, Bromelain, Calcium Hydroxide

Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
bromelain
Calcium hydroxide
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intracanal Medication

Eligibility Criteria

25 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Patients who are free from any physical or mental handicapping condition with no underlying systemic disease (ASA I or II) . Age between 25-50 years old. Males & Females. Patients who can understand pain scale and can sign the informed consent. Mandibular Single rooted premolars, having single root canal: Diagnosed clinically with pulp necrosis. Absence of spontaneous pulpal pain. Positive pain on percussion denoting apical periodontitis. Slight widening in the periodontal membrane space with or without periapical radiolucency radiographically. Normal occlusal contact with opposing teeth Exclusion Criteria: Medically compromised patients: Pain levels and healing following treatment would be compromised as these patients have shown higher incidence of pain and lower healing rate. Pregnant women: Avoid radiation exposure, anesthesia, and medication. If antibiotics have been administrated by the patient during the past 12 hours preoperatively might alter their pain perception. Patients reporting bruxism or clenching: Avoid further pressure on an already inflamed tooth inducing subsequent irritation and inflammation. Teeth that shows association with acute periapical abscess and swelling: Need special treatment steps which could involve additional visits with incision and drainage. Also, it could influence initiation and progression of postoperative pain. Greater than grade I mobility or pocket depth greater than 5mm. Need special surgical and/or periodontal therapy. No restorability: Hopeless tooth. Immature teeth. Radiographic evidence of external or internal root resorption.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    calcium hydroxide arm

    bromelain arm

    Arm Description

    intracanal medication of calcium hydroxide paste

    intracanal medication of bromelain paste (Bromelain powder with enzymatic activity of 2400 Gelatin digestion unit per Gram was mixed with saline in 1:1 proportion 1 g powder was mixed with 1 ml distilled water)

    Outcomes

    Primary Outcome Measures

    postoperative pain intensity
    measured using Numerical rating scale
    postoperative pain intensity
    measured using numerical rating scale
    postoperative pain intensity
    measured using numerical rating scale
    postoperative pain intensity
    measured using numerical rating scale

    Secondary Outcome Measures

    bacterial load reduction
    using Colony forming unit (CFU )
    enterococcal bacterial count
    using Colony forming unit (CFU )
    bacterial load reduction
    using Colony forming unit (CFU )
    enterococcal bacterial count
    using Colony forming unit (CFU )
    bacterial load reduction
    using Colony forming unit (CFU )
    enterococcal bacterial count
    using Colony forming unit (CFU )
    Incidence of inter- appointment swelling
    using binary chart (yes or no)

    Full Information

    First Posted
    December 21, 2022
    Last Updated
    January 15, 2023
    Sponsor
    Cairo University
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05687760
    Brief Title
    Effect of Bromelain Versus Calcium Hydroxide as an Intracanal Medication on the Intensity of Postoperative Pain and Bacterial Load Reduction in Necrotic Single Rooted Lower Premolars
    Official Title
    Effect of Bromelain Versus Calcium Hydroxide as an Intracanal Medication on the Intensity of Postoperative Pain and Bacterial Load Reduction in Necrotic Single Rooted Lower Premolars (A Randomized Clinical Trial)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 10, 2023 (Anticipated)
    Primary Completion Date
    February 10, 2023 (Anticipated)
    Study Completion Date
    February 10, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cairo University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    the aim of the study is to compare the effect of bromelain vs calcium hydroxide as intracanal medication on intensity of pain and bacterial load in necrotic single lower premolars
    Detailed Description
    After diagnosing the case as pulp necrosis and confirming that the patient conforms to all eligibility criteria, the operator will enroll the patient in the study. Treatment of all cases will be completed in two visits as follows : Anesthetizing the tooth using mental nerve block technique by local anesthesia of 1.8 ml of 2% Mepivacaine HCl with 1:100,000 epinephrine (Artinibsa®; Inibsa Dental, Lliçà de Vall,Spain) . Removal of Caries and/or coronal restorations completely with sterile bur and rubber dam will be applied. Cleaning the operative field, including the tooth, the clamp, and rubber dam sheet, with 3% hydrogen peroxide until no further bubbling of the peroxide occurred. All surfaces will then be disinfected by a sterile cotton swab with a 5.25% sodium hypochlorite solution. Preparation of access cavity using another sterile round carbide bur size 3 and Endo-z bur (Dentsply Maillefer, Ballaigues, Switzerland) . After completing the access, the operative field and the pulp chamber will be cleaned and disinfected once again in the same way mentioned above. NaOCl will be then neutralized with 5% sodium thiosulfate. The pre-instrumentation root canal sample (S0) will be taken as follows: a sterile paper point will be placed in the canal to soak up the fluid in the canal to a level approximately 1 mm short of the tooth apex based on diagnostic radiographs and estimated working length. The paper point will be left in the canal for at least 1 minute. Paper points will then be transferred aseptically to tubes containing sterile brain heart infusion (BHI) broth. Confirming the patency of the root canals using stainless steel hand K-files size #10 and #15(K-Files, MANI, INC., Industrial Park, Utsunomiya, Tochigi, Japan) Working length will be determined using an electronic apex locator(Root ZX, J. Morita USA, Irvine, CA) then confirmed radiographically to be 1 mm shorter than radiographic apex. Mechanical preparation will be done using M PRO rotary files in an endodontic motor (X-Smart, Dentsply Maillefer, USA) The first file (18/.09) will be used as an orifice opener for two thirds of the working length followed by (20/.04) and (25/.06) for the full working length and finally (35/.04). In-and-out motions will be applied with stroke lengths not exceeding 3 mm in the cervical, middle, and apical thirds until attaining the established WL. The first file is used with a continuous rotary motion at a speed of 500rpm and torque of 3Ncm. The second, third and fourth files are used with a speed of 300 rpm and torque of 1.5Ncm. The canal will be irrigated and recapitulated after the use of each instrument. The canal will be thoroughly irrigated with 2.5% sodium hypochlorite root canal irrigant (5ml for 1 min) using disposable plastic syringe with side vented needle gauge 30 (Steri irrigation tips; Diadent, Chungcheongbuk-do, Korea) reaching 1 mm short of the working length. All teeth will receive the same volume of irrigant (5 ml prior to instrumentation, 5 ml between each file and 5 ml as final flush after root canal instrumentation to reach a total volume of 25 ml in total). Post-instrumentation sample (S1) will be taken as previously mentioned. The patients will then be assigned into two groups : In the intervention groups, Bromelain paste (Bromelain powder with enzymatic activity of 2400 Gelatin digestion unit per Gram was mixed with saline in 1:1 proportion 1 g powder was mixed with 1 ml distilled water) will be placed inside the canals using sterile plastic syringe with needle gauge 27 without binding 1mm shorter than working length . The access cavities were closed using sterile cotton pellet and intermediate restorative material . In the control group, Ca(OH)29will be placed inside the canals using sterile plastic syringe with needle gauge 27 without binding 1 mm shorter than working length .The access cavities were closed using sterile cotton pellet and intermediate restorative material . Patients will be asked to record their pain level after the first visit on Numeric Rating Scale (NRS) at 6, 12, 24, 48 hours.(Appendix V) Each patient will be given a chart to record postoperative swelling. If swelling was recorded, the patient will be appointed for clinical examination to assess the severity by blinded assessor in a swelling rating scale and to determine if systemic antibiotics (Augmentin 625mg/8 hours/5 days) or drainage would have been needed. In the recall appointment after 1 week. Rubber dam will be applied then intracanal medication will be removed using copious irrigation and fanta AF max rotary file (#25 0.04) and tooth will be disinfected as before. The previously sampled canal will be re-entered, flushed with copious saline irrigation and a third sample (S-2) will be taken. After the sampling, final flush with 2.5% NaOCL and 17% EDTA will be done in both groups. Master cones of (0.40) taper gutta-percha(Meta Biomed Co., Ltd, Korea) will be fitted to the working length and a radiograph will be taken to ensure proper length. Obturation will be done by modified single cone technique using epoxy resin sealer(Adseal, Meta Biomed CO.,LTD, Korea)and 4% taper gutta percha cones together with auxillary cones. The tooth will be sealed by temporary restoration ,Then the details of the endodontic procedure for each patient will be recorded in the patient's procedure chart (Appendix IV) . The patient will be instructed to return to complete the treatment procedures until placing a full-coverage restoration. In case of severe pain or persisting pain patients are instructed to take prescribed analgesic (Ibuprofen 400mg), not to take it less than 6 hours apart

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Intracanal Medication, Bromelain, Calcium Hydroxide, Bacterial Load Reduction

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    calcium hydroxide arm
    Arm Type
    Active Comparator
    Arm Description
    intracanal medication of calcium hydroxide paste
    Arm Title
    bromelain arm
    Arm Type
    Experimental
    Arm Description
    intracanal medication of bromelain paste (Bromelain powder with enzymatic activity of 2400 Gelatin digestion unit per Gram was mixed with saline in 1:1 proportion 1 g powder was mixed with 1 ml distilled water)
    Intervention Type
    Biological
    Intervention Name(s)
    bromelain
    Intervention Description
    is a proteolytic enzyme derived from the stem part and fruit of pineapples (Ananas comosus).used as intracanal medication
    Intervention Type
    Drug
    Intervention Name(s)
    Calcium hydroxide
    Intervention Description
    calcium hydroxide
    Primary Outcome Measure Information:
    Title
    postoperative pain intensity
    Description
    measured using Numerical rating scale
    Time Frame
    6 hours post-instrumentation
    Title
    postoperative pain intensity
    Description
    measured using numerical rating scale
    Time Frame
    12 hours post-instrumentation
    Title
    postoperative pain intensity
    Description
    measured using numerical rating scale
    Time Frame
    24 hours post-instrumentation
    Title
    postoperative pain intensity
    Description
    measured using numerical rating scale
    Time Frame
    48 hours post-instrumentation
    Secondary Outcome Measure Information:
    Title
    bacterial load reduction
    Description
    using Colony forming unit (CFU )
    Time Frame
    immediately after access preparation and pre- instrumentation.
    Title
    enterococcal bacterial count
    Description
    using Colony forming unit (CFU )
    Time Frame
    immediately after access preparation and pre- instrumentation.
    Title
    bacterial load reduction
    Description
    using Colony forming unit (CFU )
    Time Frame
    immediately after instrumentation
    Title
    enterococcal bacterial count
    Description
    using Colony forming unit (CFU )
    Time Frame
    immediately after instrumentation
    Title
    bacterial load reduction
    Description
    using Colony forming unit (CFU )
    Time Frame
    1 week after intracanal medicament placement
    Title
    enterococcal bacterial count
    Description
    using Colony forming unit (CFU )
    Time Frame
    1 week after intracanal medicament placement
    Title
    Incidence of inter- appointment swelling
    Description
    using binary chart (yes or no)
    Time Frame
    Up to 48 hours post- operatively

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    25 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Patients who are free from any physical or mental handicapping condition with no underlying systemic disease (ASA I or II) . Age between 25-50 years old. Males & Females. Patients who can understand pain scale and can sign the informed consent. Mandibular Single rooted premolars, having single root canal: Diagnosed clinically with pulp necrosis. Absence of spontaneous pulpal pain. Positive pain on percussion denoting apical periodontitis. Slight widening in the periodontal membrane space with or without periapical radiolucency radiographically. Normal occlusal contact with opposing teeth Exclusion Criteria: Medically compromised patients: Pain levels and healing following treatment would be compromised as these patients have shown higher incidence of pain and lower healing rate. Pregnant women: Avoid radiation exposure, anesthesia, and medication. If antibiotics have been administrated by the patient during the past 12 hours preoperatively might alter their pain perception. Patients reporting bruxism or clenching: Avoid further pressure on an already inflamed tooth inducing subsequent irritation and inflammation. Teeth that shows association with acute periapical abscess and swelling: Need special treatment steps which could involve additional visits with incision and drainage. Also, it could influence initiation and progression of postoperative pain. Greater than grade I mobility or pocket depth greater than 5mm. Need special surgical and/or periodontal therapy. No restorability: Hopeless tooth. Immature teeth. Radiographic evidence of external or internal root resorption.

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Effect of Bromelain Versus Calcium Hydroxide as an Intracanal Medication on the Intensity of Postoperative Pain and Bacterial Load Reduction in Necrotic Single Rooted Lower Premolars

    We'll reach out to this number within 24 hrs