Necrosis of Pulp
Conditions
Interventions
The sixty patients who participated in the study were between 18 and 59 years old. Thirty patients were enrolled in each experimental group (n=30). Patients were randomly allocated into two groups thr
E06.397
Sponsors
Fabiana Menezes Galdino de Aragao
Centro de Pesquisas Odontologicas São Leopoldo Mandic
Faculdade São Leopoldo Mandic
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Healthy volunteers; both sexes; age above 18 years
Exclusion criteria
Exclusion criteria: Pregnancy; diabetics; immunosuppressed patients; under 18 years old
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Pain would be statistically similar across all study times;Endpoint found 1: The results were submitted to statistical tests of association and Student's t test. The number of participants who reported pain was statistically similar, both in 24h and 48h. At 72h and 7 days, no participant from any of the experimental groups reported pain. There was no statistically significant difference in pain intensity between experimental groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: The amount of analgesic pills ingested by the participants would be statistically similar in the two studied groups.;Endpoint found 2: There was no statistically significant difference in the comparison between the experimental groups for the amount of pills consumed for pain relief in any of the evaluated times | — |
Countries
Brazil
Contacts
Public ContactFabiana Aragao
Faculdade São Leopoldo Mandic
Outcome results
None listed