2017
DOI: 10.1111/iej.12795
|View full text |Cite
|
Sign up to set email alerts
|

The effect of preoperative oral administration of prednisolone on postoperative pain in patients with symptomatic irreversible pulpitis: a single‐centre randomized controlled trial

Abstract: Preoperative oral administration of a single dose of 40 mg prednisolone was beneficial to control short-term post-obturation pain after single-visit root canal treatment in patients with symptomatic irreversible pulpitis reducing pain incidence after 24 h by approximately 30% and postoperative analgesic intake by approximately 55%.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
36
0
1

Year Published

2018
2018
2024
2024

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 16 publications
(37 citation statements)
references
References 27 publications
0
36
0
1
Order By: Relevance
“…Of those 45 references, fourteen were eligible to be included in qualitative analyses [ 14 15 20 21 22 23 24 25 26 27 28 29 30 31 ]. The reasons for exclusion after full-text were that the intervention was a combination of corticosteroid and antibiotic (n = 8), no endodontic treatment (n = 7), no corticosteroid (n = 8), no pain outcome (n = 1), no post- endodontic pain outcome- pain during anesthesia (n = 1) [ 32 ], no control group (n = 1), different intervention (n = 3), no placebo/no treatment group (n = 1) and a review/systematic review of the literature (n = 1).…”
Section: Resultsmentioning
confidence: 99%
See 4 more Smart Citations
“…Of those 45 references, fourteen were eligible to be included in qualitative analyses [ 14 15 20 21 22 23 24 25 26 27 28 29 30 31 ]. The reasons for exclusion after full-text were that the intervention was a combination of corticosteroid and antibiotic (n = 8), no endodontic treatment (n = 7), no corticosteroid (n = 8), no pain outcome (n = 1), no post- endodontic pain outcome- pain during anesthesia (n = 1) [ 32 ], no control group (n = 1), different intervention (n = 3), no placebo/no treatment group (n = 1) and a review/systematic review of the literature (n = 1).…”
Section: Resultsmentioning
confidence: 99%
“…The gender and age of the study groups is listed in Table 1 . Eight studies specified their gender ratio of their samples and F/M ratio varied from 0.9 to 2.3 [ 14 15 20 21 23 26 27 31 ] with a majority of females in most of the studies. The age of the participants was between 18 to 71 ( Table 1 ).…”
Section: Resultsmentioning
confidence: 99%
See 3 more Smart Citations