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In both groups, the intervention continued with rinsing of the implant surface with an abundant amount of sterile saline for 1 min.
For both groups the intervention period is 14 weeks.
Although similar pain intensities were perceived by patients in both groups, the intervention group had a better ambulatory status at discharge (p < 0.001) (Table 5).
Subsequently, the GPs of both groups (the intervention group trained, the control group not) will audio- or videotape one of their yearly consultations with a T2DM patient.
The study design was unable to determine the route that increased rape reporting: knowledge increased in both groups, the intervention did not significantly change attitude.
However, when this analysis was repeated on baseline data for both groups, the intervention group reported lower scores on both SF-12 MCS (z = -5.76, p < 0.001) and social activity scores (z = -4.12, p < 0.001) compared with controls.
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While condom sales were decreasing in both study groups, the intervention appeared to stem the reduction in sales in the intervention pharmacies, particularly independent pharmacies.
There was no significant difference between QOL mean score of both groups before the intervention, however the QoL significantly improved in the experimental group after the intervention (P= 0.001), while the QoL decreased in control group.
In comparison with the DMH only group, both the intervention groups significantly reduced the number of ACs and ACF (p-value < 0.001 for 250 mg/kg vs. DMH only; p-value < 0.0001 for 500 mg/kg vs. DMH only).
At T2, 6 months after T1, retention of knowledge was measured by administering the knowledge test to both groups, whereas the intervention group also completed the applicability questionnaire.
Both groups, the control and the intervention, lacked blinding and placebo designs.
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both groups the dosage
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both groups the grade
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both groups the norepinephrine
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