Intervention not reported
Physiologic measurements of systemic absorption at 1 year' · participants with glaucoma or ocular hypertension
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
Escalation of therapy at 1 year' · participants with glaucoma or ocular hypertension
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
Mean change in visual fields at 1 year' · participants with glaucoma or ocular hypertension
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 events at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Preterm birth < 35 weeks · Pregnant women considered to have periodontal disease (gingivitis or periodontitis) after dental examination
1 finding from 1 review
Probing pocket depth · Pregnant women considered to have periodontal disease (gingivitis or periodontitis) after dental examination
Periodontal treatment (scaling and root planing, alone or with… led to lower probing depth compared with alternative (less intensive) periodontal treatment, alone or with…; GRADE not reported.
1 finding from 1 review
Small‐for‐gestational age · Pregnant women considered to have periodontal disease (gingivitis or periodontitis) after dental examination
The review found no eligible studies for this question.
1 finding from 1 review
Pain (short‐term) Pain index1. Scale from: 0 to 70. · participants with acute or subacute low‐back pain
1 finding from 1 review
Duration of sick‐leave Sick‐leave > 21 days · participants with acute or subacute low‐back pain
It is very uncertain whether back school changes duration of sick‐leave Sick‐leave > 21 days compared with short‐wave diathermy at the lowest intensity (very low certainty).
1 finding from 1 review
Intervention not reported
Clinical outcome: systolic blood pressure (automated sphygmomanometer or electronic pressure monitor) ATCS Plus or IVR versus usual care at median · patients with hypertension
1 finding from 1 review
Intervention not reported
Clinical outcome: diastolic blood pressure (automated sphygmomanometer and electronic cuff) ATCS Plus, unidirectional versus usual care at median · patients with hypertension
1 finding from 1 review
Intervention not reported
Clinical outcome: blood pressure control, 26 weeks Multimodal/complex interventionf versus usual care · patients with hypertension
1 finding from 1 review
Intervention not reported
Clinical outcome: Health statush, depressioni, 6 weeks ATCS Plus versus enhanced usual care (plus information) · patients with hypertension
1 finding from 1 review
Intervention not reported
Behavioural outcome: medication use Multimodal/complexk, ATCS Plus versus usual care or enhanced usual care (plus information) · patients with hypertension
1 finding from 1 review
Intervention not reported
Behavioural outcome: physical activity levels, 12 weeks IVR versus enhanced usual care · patients with hypertension
1 finding from 1 review
Intervention not reported
Adverse outcome: unintended adverse events attributable to the intervention Multimodal/complex intervention, ATCS Plus, IVR, unidirectional ATCS versus various controls · patients with hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
HRQOL ‐ not measured · Participants with rosacea
The review found no eligible studies for this question.
1 finding from 1 review
Participant‐assessed improvement in rosacea severity · Participants with rosacea
1 finding from 1 review
Proportion of participants with adverse event Pain as · Participants with rosacea
1 finding from 1 review
Physician‐assessed improvement in rosacea severity ‐ not measured · Participants with rosacea
The review found no eligible studies for this question.
1 finding from 1 review