Postoperative Pain After Dental Post Application

Medipol Health Group

Status: Completed

Conditions: Postoperative Pain; Vibration; Exposure; Endodontically Treated Teeth

Treatments: Procedure: Group 2: two-visit RCT; Procedure: Group 1: single-visit RCT

Study type: Interventional

Funder types: Other

Identifiers

NCT03942107

dental posts postop pain

Details and patient eligibility

About

In this study the effect of dental post application on postoperative dental pain in patients with asymptomatic teeth after a single-appointment root canal treatment will be evaluated.

Full description

The aim of this clinical study is to evaluate the effect of dental post application on postoperative pain intensity level in patients with asymptomatic teeth after a single-appointment root canal treatment. A total of one hundred patients with asymptomatic teeth and with no contradictory medical history who are indicated for non-surgical root canal treatment and application of a dental post at the Endodontic Clinic, Faculty of Dentistry, Istanbul Medipol University, between April and December of 2019 will be included. All of the patients will be recruited from the Istanbul Medipol University Dental Clinics in Istanbul. the patients will be divided in two groups (n=50). Consent will be obtained from all study participants before the treatment. After the root canal treatments are completed in single-visit, in the first groups dental posts will be applied immediately at the same visit and patients will be appointed for pain assessment. In group 2 after the root canal treatment a temporary filling be applied in the access cavity and patients will be appointed for pain assessment. Dental posts will be applied after the pain assessment is completed at the end of 1 week. All treatments will be performed by one endodontist. Postoperative pain intensity will be assessed at 24, 48, and 72 h; 7 days; after the treatment. The teeth will be examined according to postoperative pain intensity levels,

Enrollment: 100 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• patients with asymptomatic teeth which were in need of orthograde non-surgical root canal treatment with post application

Exclusion criteria

Patients

• 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

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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100 participants in 2 patient groups

Group 1: RCT+post+core in 1 visit

Active Comparator group

Description:

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.

Treatment:

Procedure: Group 1: single-visit RCT

Group 2: after RCT, post and core in 2nd visit

Active Comparator group

Description:

after root canal treatment conducted with 2Shape NiTi system, the postoperative pain evaluation will be completed prior applying post and core for coronal restoration.

Treatment:

Procedure: Group 2: two-visit RCT