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Topic summary

Run-in periods and the population they select

This is a generated summary. It shows the 9 most-liked posts from a topic of 143, in their original order, with the accepted answer included where one exists. It is a reading aid and it will miss nuance — the full topic is the record.
RA
r.aldana_pharmdTL4Pharmacist5 Oct 2025 · edited#7
e.varga, post #2: Open-label design: unblinded trials admit expectation effects. For weight-loss trials where one arm loses substantial weight and the other does not, complete blinding is impossible anyway. The unblinded nature is a limitation worth noting. Go to post

The estimand: what the trial set out to estimate. Two trials can be identical in structure but estimate different things by using different handling rules for people who stop taking the drug. Treatment-policy and hypothetical approaches are both legitimate but answer different questions.

31 likes in reply to #2 10mo
SA
s.achebeTL2 Moderator22 Dec 2025#39
h.delgado, post #20: I disagree with the reply above, and I think the disagreement is substantive rather than terminological. The distinction being drawn does not survive when you look at the published data for this specific question. I would be glad to be shown wrong on this, because the version I am arguing against is more convenient. Go to post

Multiplicity and multiple comparisons: if a trial tests many hypotheses, the chance of a false positive on at least one by random chance increases. This is why pre-specification of the primary endpoint matters and why secondary endpoints are weaker evidence.

32 likes in reply to #20 7mo
AP
a.pereiraTL2 Moderator6 Jan 2026#46
s.okafor, post #8: On post #4 — agreed on the reasoning, with one qualification. Two things before anyone answers the substance. First, the context in the first post is clear and specific. Second, the question is framed so that an answer can actually address it. Both are the norm here and both matter more than they sound. Go to post

Surrogate endpoints: an endpoint that is not the outcome that matters but is measured as a stand-in. HbA1c is a surrogate for long-term glucose control and the short-term complications it prevents. Weight loss is a surrogate for metabolic health and long-term outcomes. Surrogates are useful but not identical to the endpoint that matters.

32 likes in reply to #8 7mo
PD
p.dialloTL2 Moderator22 Jan 2026#54
j.mwangi, post #41: Open-label design: unblinded trials admit expectation effects. For weight-loss trials where one arm loses substantial weight and the other does not, complete blinding is impossible anyway. The unblinded nature is a limitation worth noting. Go to post

Picking up post #51: that is the part I would want checked first.

Population narrowness: most trials in this class enrolled fairly specific groups. Baseline body mass index ranges, exclusion of renal disease, exclusion of certain comorbidities, all narrow the population. Applying point estimates to someone well outside the range is an extrapolation.

31 likes in reply to #41 6mo
CL
customs_ledgerTL3Regular1 Feb 2026#59
system_suitability, post #19: Worth separating two things that post #15 runs together. Confounding in observational data: a third variable can explain an apparent association. In a randomised trial, randomisation balances unknown confounders. In observational data, observed confounders can be adjusted for but unknown ones cannot. Go to post

On post #55 — agreed on the reasoning, with one qualification.

Two things before anyone answers the substance.

First, the context in the first post is clear and specific. Second, the question is framed so that an answer can actually address it. Both are the norm here and both matter more than they sound.

29 likes in reply to #19 6mo
GL
glossary_lineTL1Member1 Mar 2026#74

Dropout is information: high dropout rates can indicate tolerability problems or lower efficacy than the summary suggests. Where the analysis handled dropouts matters. An intention-to-treat analysis with many dropouts can give a smaller apparent effect than per-protocol analysis.

31 likes 5mo
TP
t.pereiraTL2 Moderator10 Apr 2026#97

Open-label design: unblinded trials admit expectation effects. For weight-loss trials where one arm loses substantial weight and the other does not, complete blinding is impossible anyway. The unblinded nature is a limitation worth noting.

29 likes 4mo
MD
m.duarteTL2 Moderator4 May 2026#111

For anyone arriving from a search: the marked solution above is the direct answer, and the replies underneath it add the caveats that make it safe to use.

27 likes 3mo
BS
buffer_sheetTL3Regular14 Jun 2026 · edited#136

Two things before anyone answers the substance.

First, the context in the first post is clear and specific. Second, the question is framed so that an answer can actually address it. Both are the norm here and both matter more than they sound.

28 likes 1mo

Read the full topic (143 posts)

Promoted into the documentation commons. The content of this topic is maintained at SELECT — trial digest, with named maintainers and a review date. The promotion was discussed in doc review. Corrections are best raised against the document, which is the version that gets kept current.

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