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Although the data were derived from randomised controlled trials, weight gain was not considered by randomisation group, and therefore we treated the data as observational.
In clinical trials, weight loss reduces the risk of diabetes in people with prediabetes (3); however, long-term weight maintenance has proven elusive.
89 In two 36-week trials, weight loss achieved with phentermine was up to 13% of initial body weight, reflecting its high efficacy.
In active controlled trials, weight gain was reported as an adverse event less often than when it was measured as an outcome of the trial, both for atypical antipsychotic (mainly olanzapine) and active control (divalproex, lithium, and lamotrigine) (Table 7).
Here again, in many trials, weight loss was far less than what would have been expected based on cumulated SSB energy deficit, suggesting either low compliance to SSB restriction or compensatory increase in total energy intake.
In some of these trials, weight loss appears to have reached a plateau by 12 20 weeks of treatment, 73, 75, 77 whereas in another study, weight loss was progressive for up to 26 weeks.
Similar(53)
In both cases, the LFP-derived PC2 single trials weights explain additional variance as this value-to-choice transformation occurs.
Throughout the trial, weight gain (g) was monitored.
On the 1st and 60th day of feeding trial, weight measurement was taken using an electronic balance (Citizen, India).
At the end of the 8-week feeding trial, weight gain, feed efficiency, feed intake and tissue proximate composition were not significantly affected by dietary CLA.
At the end of the feeding trial, weight gain, specific growth rate, feed efficiency and protein efficiency ratio of fish fed SG and SG + BG were significantly higher than those of fish fed the BG and CONT diets (P < 0.05).
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