Failure to correct the anterior open bite (open bite not closed) · Children and adolescents (over 80% aged 16 years or younger at treatment start) with anterior open bite (lack of vertical overlap or…
Removable appliance with palatal crib associated with high-pull… led to lower failure to correct the anterior open bite (open bite not closed) compared with no treatment; GRADE not reported.
1 finding from 1 review
Intervention not reported
At least 50% reduction in pain or equivalent · adults with complex regional pain syndrome type 1 (lower limb)
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
At least 30% reduction in pain · adults with complex regional pain syndrome type 1 (lower limb)
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Proportion below 30/100 mm on VAS · adults with complex regional pain syndrome type 1 (lower limb)
1 finding from 1 review
no estimate extracted
19 participants
Very low
Intervention not reported
Patient Global Impression of Change: much or very much improved · adults with complex regional pain syndrome type 1 (lower limb)
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Adverse event withdrawals · adults with complex regional pain syndrome type 1 (lower limb)
1 finding from 1 review
no estimate extracted
20 participants
Very low
Intervention not reported
Serious adverse events · adults with complex regional pain syndrome type 1 (lower limb)
1 finding from 1 review
no estimate extracted
20 participants
Very low
Intervention not reported
Death · adults with complex regional pain syndrome type 1 (lower limb)
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Adverse effects · Participants with a previous or current history of recurrent aphthous stomatitis (RAS), diagnosed on history and clinical examination;…
1 finding from 1 review
Effectiveness · Participants with a previous or current history of recurrent aphthous stomatitis (RAS), diagnosed on history and clinical examination;…
1 finding from 1 review
Deaths · patients with acute organophosphate pesticide poisoning
It is very uncertain whether higher dose changes deaths compared with lower dose (very low certainty).
1 finding from 1 review
Intermediate syndrome · patients with acute organophosphate pesticide poisoning
It is very uncertain whether higher dose changes intermediate syndrome compared with lower dose (very low certainty).
1 finding from 1 review
Ventilated · patients with acute organophosphate pesticide poisoning
It is very uncertain whether higher dose changes ventilated compared with lower dose (very low certainty).
1 finding from 1 review
Intervention not reported
mg/day LDL cholesterol · participants with normal or abnormal lipid profiles
The intervention showed no clear difference in mg/day LDL cholesterol (high certainty).
1 finding from 1 review
Intervention not reported
mg/day LDL cholesterol · participants with normal or abnormal lipid profiles
The intervention showed no clear difference in mg/day LDL cholesterol (moderate certainty).
1 finding from 1 review
Intervention not reported
mg/day LDL cholesterol · participants with normal or abnormal lipid profiles
The intervention showed no clear difference in mg/day LDL cholesterol (moderate certainty).
1 finding from 1 review
Intervention not reported
mg/day LDL cholesterol · participants with normal or abnormal lipid profiles
The intervention showed no clear difference in mg/day LDL cholesterol (high certainty).
1 finding from 1 review
Intervention not reported
Pravastatin 10 to 80 mg/day (6 to 156 weeks) · participants with normal or abnormal lipid profiles
The review found no eligible studies for this question.
1 finding from 1 review
Intervention not reported
WDAEs · participants with normal or abnormal lipid profiles
It is very uncertain whether the intervention changes WDAEs (very low certainty).
1 finding from 1 review
Underweight · healthy, full‐term (37 to 42 weeks), formula‐fed infants
1 finding from 1 review