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Patient intraoperative discomfort after using rotary or reciprocating systems

Patient intraoperative discomfort after using rotary or reciprocating systems: a prospective and randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11624674
Enrollment
23
Registered
2016-04-14
Start date
2015-01-01
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Endodontic disease Oral Health

Interventions

After local anesthesia with 2% lidocaine with 1:100,000 epinephrine, a rubber dam was placed and the access cavity was prepared using sterile diamond burs. If patients recorded any pain sensation duri
J. Morita Corp., Tokyo, Japan). Working length (WL) was established by deducting 1 mm from the canal length. Only cases where a 10-K file go passively and a 15-K file did not got passively to the WL i
mesiobuccal and mesiolingual canals for mandibular molars) were selected. These cases were classified as small and R25 was recommended, according to the manufacturer´s protocol. All teeth received the

Sponsors

National Council for Scientific and Technological Development (Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy (ASA I) adults older than 18 years of age that had been admitted to the Endodontics Department of FOP-UNICAMP, from January 2015 to December 2015 with a clinical diagnosis of irreversible pulpitis or necrosis in the first or second maxillary and mandibular molars 2. Pulpal status that has been confirmed by a cold test

Exclusion criteria

Exclusion criteria: 1. Taking any medication that could alter their perception of pain (analgesic or non steroidal anti-inflammatory drugs) 2. Radiographic findings that included absence of periapical radiolucency except for a widened periodontal ligament

Design outcomes

Primary

MeasureTime frame
Intraoperative discomfort, measured using the visual analogue score (VAS), during the procedure, between the two different instrumentation groups

Countries

Brazil

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026