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No statistically significant differences were seen between the medication groups for the main outcome measures (IBS SSS and IBS-QOL) at 6 or 12 weeks.
No significant difference was found in HADs, Enablement or SGA between the medication groups or in the HADs scores between the website groups (Tables 4 and 7).
All DMSRQ-SF scales differentiated between the medication groups, with insulin users consistently having fewer positive scores than one or both of the other medication groups.
The lack of difference between the medication groups may be due to low power with the limited numbers in this trial.
Crichton et al. reported tear film instability in patients with open-angle glaucoma and ocular hypertension after 12-week treatment with different preservative prostaglandin analogs, but with no differences in TBUT between the medication groups (TBUT in seconds: bimatoprost with 0.02% BAK 9.7 ± 5.7; latanoprost with 0.02% BAK 9.3 ± 4.0; P = 0.379) [ 31].
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The mean ΔYKL-40, Δ %FEV1 and ΔACT values differed significantly between the two medication groups.
There were no significant differences between the two medication groups.
This score is used to weight individuals differently to achieve balance in covariates at baseline between the four medication groups (metformin/no statin, metformin + statin, no metformin/no statin, no metformin + statin); therefore, potential confounding due to pretreatment characteristics is minimized and data from an observational study can be causally interpreted.
The authors found no difference between the antiplatelet medication group and the no antiplatelet group with regard to volume of ICH on CT, haematoma growth or outcome score.
Latency did not differ between the three SCZ medication groups.
Between medication groups the PPV differed significantly: children on combination therapy were more likely to have doctor-diagnosed asthma.
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