Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2019-04-05
2019-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SCREENING
NONE
Study Groups
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Group 1: RCT+post+core in 1 visit
the root canal treatment will be completed with 2Shape NiTi system as well as post and core application in the same visit prior to postoperative pain evaluation.
Group 1: single-visit RCT
both root canal treatment and post and core restoration of the coronal part of the tooth is completed in single visit prior to postoperative pain evaluation at 24, 48 and 72-h and 7-day follow-up time
Group 2: after RCT, post and core in 2nd visit
after root canal treatment conducted with 2Shape NiTi system, the postoperative pain evaluation will be completed prior applying post and core for coronal restoration.
Group 2: two-visit RCT
after root canal treatment is completed, postoperative pain evaluation will be conducted in this group at 24, 48 and 72-h and 7-day follow-up time. post-core application will be completed at the seventh day after postoperative pain evaluation.
Interventions
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Group 1: single-visit RCT
both root canal treatment and post and core restoration of the coronal part of the tooth is completed in single visit prior to postoperative pain evaluation at 24, 48 and 72-h and 7-day follow-up time
Group 2: two-visit RCT
after root canal treatment is completed, postoperative pain evaluation will be conducted in this group at 24, 48 and 72-h and 7-day follow-up time. post-core application will be completed at the seventh day after postoperative pain evaluation.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* who were younger than 18 years old,
* who had contradictory medical history for root canal treatment,
* who used antibiotics 1 month prior and analgesics 1 week prior to the treatment,
* who could not abide the follow-up time Teeth
* that were symptomatic
* with previous root canal treatment
* with present or suspected vertical root fracture
* with ≥ 4 mm periodontal pocket depth
* with apical lesions ≥ 5mm
* with damaged or resorbed apex
* that were in need of apical surgery
18 Years
60 Years
ALL
Yes
Sponsors
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Istanbul Medipol University Hospital
OTHER
Responsible Party
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Tan Firat Eyuboglu
Assistant Professor, Head of Department of Endodontics
Principal Investigators
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TAN F EYUBOGLU, DDS,PhD
Role: PRINCIPAL_INVESTIGATOR
Medipol University
Locations
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Istanbul Medipol University School of Dentistry
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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dental posts postop pain
Identifier Type: -
Identifier Source: org_study_id
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