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Comparison of single-dose preoperative Ibuprofen vs. Ibuprofen with Arginine in the control of postoperative pain in canal treatments

Preoperative single-dose comparison of Ibuprofen versus Ibuprofen with Arginine in postoperative pain control in Endodontics: Double-blind, randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5tfrhv
Enrollment
Unknown
Registered
2018-11-08
Start date
2018-09-05
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

Arginine

Interventions

Oral ibuprofen (400 mg) was administered to a group of 30 volunteers in the preoperative period of endodontic instrumentation in asymptomatic teeth, ibuprofen with arginine (400 mg) orally for a group
Drug

Sponsors

Universidade Estadual de Ponta Grossa
Lead Sponsor
Centro de Ensino Superior dos Campos Gerais
Collaborator

Eligibility

Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Men or women between 20 and 59 years of age in good health; Satisfy ASA I or II medical history according to the American Society of Anesthesiologists; Need for endodontic therapy in uni or multi-root teeth, asymptomatic with necrotic pulp; Volunteers who can provide informed consent.

Exclusion criteria

Exclusion criteria: Men or women under 20 years of age; Pregnant or lactating women; History of allergy or hypersensitivity to ibuprofen, arginine or local anesthetics; Need for antibiotic prophylaxis; Gastrointestinal disorders, esophageal reflux; Active asthma; Decreased hepatic function; Bleeding disorders; Decompensated diabetes mellitus; Ingestion of analgesics and anti-inflammatories in the last 12 hours (as it may exert a therapeutic effect at the time of the study); Intake of alcoholic beverage in the last 24 hours;Individuals classified as class III to V according to the American Society of Anesthesiologists; Individuals unable to provide informed consent.

Design outcomes

Secondary

MeasureTime frame
The use of the drugs is expected to interfere positively in the quality of life and decrease of the anxiety of the volunteers. Quality of life will be measured using the OHIP-14 questionnaire and the anxiety will be measured using the IDATE-T and IDATE-E questionnaires.

Primary

MeasureTime frame
It is expected that there is a significant difference between the use of ibuprofen with arginine compared to conventional ibuprofen and placebo in the control of pain after endodontic instrumentation. Verified through the use of numeric pain scale (ENSR).

Countries

Brazil

Contacts

Public ContactAmanda Fischborn

Universidade Estadual de Ponta Grossa

amandafischborn@hotmail.com55042998020784

Outcome results

None listed

Source: REBEC (via WHO ICTRP)