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Our protocol involved four sets of five contractions of 10 seconds' duration each (total approximately 4 minutes) at 30%and5050% MVC, which differs from the protocols used in other studies, 16, 18, 26, 43– 45 in which four series of contractions for 2 minutes each, totaling approximately 8 minutes, were used.
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This differs from the protocol where the recommended cell size is 5′ × 5′.
The protocol P2 differs from the protocol P1 in that, in the latter, the source does not transmit during the second time slot, irrespective to whether the relay is active or not during the second time slot.
Nevertheless, the study protocol differs from the protocol in the present investigation; the imiquimod cream was administered four weeks after the PDT and the patients completed only one session of imiquimod.
Methods reported in publications differed from the protocol for 39/49 trials.
Overall, 25 publications that described the statistical test for primary outcome measures differed from the protocol (figure, box 2).
None of the patients received additional tobramycin suppositories or tobramycin nebulization, and in none of the patients, tobramycin dose differed from the protocol.
28 29 30 We identified two types of discrepancies: lack of pre-specification, where published information about the sample size calculation or data analysis methods did not appear in the protocol; and unacknowledged amendments, where published information differed from the protocol.
This differs from the existing protocols, in which the first session is used for mutual goal setting.
These protocols differ from the former protocols in that they are simpler, e.g., they omit features such as quality of service guarantees, and offer collision prevention.
This protocol differs from the 1 1 training protocol in only one way: a group of 4 6 individuals are supervised by a CEP at each session.
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