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Comparison of the analgesic effect between acupuncture and dipyrone in acute tooth pain

Comparative analgesia between acupuncture and dipyrone in acute tooth pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8sxw2r
Enrollment
Unknown
Registered
2018-06-25
Start date
2018-02-23
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

Acute tooth pain

Interventions

Intervention 1 (real acupuncture group): performing an acupuncture session using points LI4, ST44 and CV23 and YinTang - 22 participants - duration: 20 minutes Intervention 2 (sham acupuncture group):
Procedure/surgery
Other
H02.004

Sponsors

Faculdade de Odontologia de Piracicaba - Universidade Estadual de Campinas (Unicamp)
Lead Sponsor
Faculdade de Odontologia de Piracicaba - Universidade Estadual de Campinas (Unicamp)
Collaborator

Eligibility

Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Adult subjects; ages 18-45; of both sexes who are not using any type of pain medication in the last 12 hours with complaint of acute tooth pain of pulp origin equal to or greater than 4 in VAS; non-allergic to dipyrone.

Exclusion criteria

Exclusion criteria: Patient under 18 years of age; pregnant women; acute tooth pain of less than 4 VAS intensity; toothache of non-pulp origin; volunteers who are using some type of pain medication; allergic to dipyrone.

Design outcomes

Primary

MeasureTime frame
Check the reduction of the intensity of the toothache after treatment with acupuncture or dipirone, evaluated through a subjective pain scale.

Secondary

MeasureTime frame
Check if there is a reduction of the concentration of the hormone cortisol in saliva after treatment with acupuncture and dipirone, evaluated through a laboratory test.

Countries

Brazil

Contacts

Public ContactMaria da Luz Sousa

Faculdade de Odontologia de Piracicaba - Universidade Estadual de Campinas (Unicamp)

luzsousa@fop.unicamp.br+55-019-2106-5209

Outcome results

None listed

Source: REBEC (via WHO ICTRP)