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Six studies reported greater improvements for intervention patients than control patients [ 4, 46- 48, 50, 58], and one study [ 64] reported great scores compared to baseline at the final follow-up point.
The combination group had a significantly reduced CRT from the monotherapy group from baseline at the final visit (−45 µm in combination group vs −30 µm in bevacizumab group, P=0.03).
There was no significant correlation between the total number of intravitreal injections during the study period and the IOP change from baseline at the final visit for patients in the total study population or in either subgroup.
As a primary outcome of gaining 15 letters or more from baseline at the final visit, a significant difference was found between the two treatment arms and the sham injection (22.2% for the 0.7 mg DEX implant, 18.4% for the 0.35 mg DEX implant, and 12% for the sham; P≤0.018).
A subset of 41 patients (21 men and 20 women) were chosen and 40 were interviewed in-depth at baseline (at the final enrollment visit before patients had started medication), at three and six months, and at 36 months after initiation of treatment.
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The measurements recorded at baseline and at the final visit were used in the analysis.
The EESC was administered at baseline and at the final study week.
Subjects' self-administered vaginal swabs were collected at baseline and at the final study visit.
Photographs of hands were obtained at baseline and at the final follow-up clinic visit.
This procedure takes 3 minutes and will be done at baseline and at the final visit.
Plasma creatinine was measured in SENIORS participants at baseline and at the final follow-up visit.
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