Cochrane · intervention · CD011930
Interventions for treating post‐extraction bleeding
Kumbargere Nagraj, S, Prashanti, E, Aggarwal, H, et al. · Cochrane Database of Systematic Reviews · 2018 · Cochrane Library
Full textEvery question was extracted from the full review (methods and results), not only its Summary of Findings table.
Questions
4
current version
GRADE rated
0
No studies
4
Included studies
0
as reported
No studies 4 · 100%Ungraded 0 · 0%Very low 0 · 0%Low 0 · 0%Moderate 0 · 0%High 0 · 0%
Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.
Review question
| Element | Planned (methods) | Found (results) |
|---|---|---|
| Population | Trials with participants of any age and either gender, who reported PEB, regardless of the type of teeth (anterior or posterior, mandibular or maxillary) | Not specified |
| Intervention | Any surgical or non‐surgical technique or material used for the treatment of PEB | Not specified |
| Comparison | Direct comparisons of different interventions/Intervention versus placebo or no treatment | Not specified |
| Outcomes | Bleeding measured by amount of blood loss, complete cessation of bleeding as assessed clinically by the investigator, time required for the control of bleeding; Patient‐reported outcomes related to pain or discomfort during the procedure; Treatment‐associated average cost; Adverse effects | Not specified |
| Study designs | Randomised controlled trials (RCTs) evaluating any intervention for treating post‐extraction bleeding (PEB). Excluded quasi‐RCTs, cross‐over trials and preventive trials. Split‐mouth studies included provided there was no possibility of contamination | Not specified |
| Timing | Not reported | Not specified |
Search date: 2018-01. Databases: Cochrane Oral Health's Trials Register; Cochrane Central Register of Controlled Trials (CENTRAL); MEDLINE Ovid; Embase Ovid; CINAHL EBSCO; US National Institutes of Health Ongoing Trials Register ClinicalTrials.gov; World Health Organization International Clinical Trials Registry Platform
Questions and results
Show all 3 versionsAny surgical or non-surgical technique or material used for the treatment of post-extraction bleeding vs Another active intervention, placebo, or no treatment
Population: People of any age and either gender with post-extraction bleeding, regardless of type of teeth (anterior or posterior, mandibular or maxillary)
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Bleeding, as measured by: amount of blood loss; complete cessation of bleeding as assessed clinically by the investigator; time required for the control of bleeding | No data are available as no RCTs have been conducted on interventions to treat post-extraction bleeding | 0 studies | No studies |
Patient-reported outcomes related to pain or discomfort during the procedure | No data are available as no RCTs have been conducted on interventions to treat post-extraction bleeding | 0 studies | No studies |
Adverse events | No data are available as no RCTs have been conducted on interventions to treat post-extraction bleeding | 0 studies | No studies |
Treatment-associated average cost | No data are available as no RCTs have been conducted on interventions to treat post-extraction bleeding | 0 studies | No studies |