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Assessment of pain after adjustment occlusal in root canal treatment

Assessment of postoperative pain after adjustment occlusal in endodontic treatment: a randomized, controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-377483
Enrollment
Unknown
Registered
2017-01-16
Start date
2016-10-17
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulpitis

Interventions

Will be included 82 individuals aged 18 to 60 years of both sexes diagnosed with irreversible Pulpitis. Patients randomized into 2 groups with 41 participants in each group through the Sealed Envelope
Procedure/surgery

Sponsors

Universidade Federal do Amazonas (UFAM)
Lead Sponsor
Universidade Federal do Amazonas (UFAM)
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Healthy patients of both sexes (male and female) aged between 18 and 60 who have root canal treatment indication in molars permanent, diagnosed with irreversible pulpitis; presence of occlusal contact prior to endodontic treatment; presence of natural or artificial opposing tooth in the occlusal contact in treated endodontically teeth; to have phone number to contact.

Exclusion criteria

Exclusion criteria: Pregnant women, patients aged less than 18 and greater than 60 years, patients taking some anti-inflammatory medication or antibiotic treatment at the time, immunocompromised, with hypersensitivity to nonsteroidal anti-inflammatory; previous diagnosis of bruxism or clenching; absence of natural or artificial tooth opposite to the tooth to be treated endodontically; complications endodontic type: calcifications, external or internal resorption, partial formation of the apical apex with dental drilling, with longitudinal or vertical fractures and severe periodontal disease; treatments in multiple sessions; patients without phone contact.

Design outcomes

Primary

MeasureTime frame
Presence or absence of postoperative pain in endodontic treatment using WaveOne® system and performing occlusal adjustment, which will be checked by a scale measuring pain, verbal description, a reduction of 30% of the expected pain after treatment endodontic using only the Wave One® system and the results will be presented by percentages

Secondary

MeasureTime frame
Will not be evaluated

Countries

Brazil

Contacts

Public ContactElizângela Barbosa Viana

Universidade Federal do Amazonas (UFAM)

elizcbarbosa@hotmail.com55-92-31844506

Outcome results

None listed

Source: REBEC (via WHO ICTRP)