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c/trialwatch·posted 9 months ago by u/aurel_mwangi

why does nobody talk about SELECT

Trial Data Receipts ×7 Sourced ×2 Long Haul ×2

Asking properly rather than in a comment on somebody else’s thread: why does nobody talk about SELECT.

Compared myself to a trial mean for about six months before realising the trial arm had dietitian contact every fortnight.

The discontinuation numbers were the most useful thing in the paper for me and they were in a supplementary table.

Went looking for the registered protocol to see whether the endpoint had changed. It had not, which was reassuring and worth checking.

Happy to answer the boring questions. Those are usually the ones worth asking.

3,491 up / 628 down85% upvoted22 commentsid 4yrmwd1 Nov 2025

22 comments

14 in this archive, depth 4

best — the order this archive was captured in

u/draw_up_dizzy282 points·9 months ago

discontinuation rate is a result, not a footnote

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u/aurel_mwangiOP201 points·8 months ago

Started keeping the trial identifiers straight in a note file because I kept mixing up two programmes in the same sentence.

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u/aurel_mwangiOP-31 points·8 months ago

open-label extensions are not the same evidence as the randomised phase

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u/adaeze_weiss137 points·8 months ago·edited

Correction: SURMOUNT is the obesity programme and SURPASS is the diabetes one. The figure you quoted belongs to the other one.

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u/yannick_salinas110 points·8 months ago

Small fix — that was the cardiovascular outcomes trial, so weight was a secondary endpoint and the population was different.

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u/trialwatch_theotrial nerd293 points·8 months ago

How to read one of these papers in fifteen minutes, in the order that actually helps.

Start with the registered protocol and check the primary endpoint against what is reported. Then the methods: who was included, what the comparator was, how long the randomised phase ran. Then the discontinuation numbers, which are a tolerability result and are usually in a supplementary table.

Only then the efficacy figure, and read the interval rather than the point estimate. Finish with the limitations section, which is where the authors say what they actually think.

Fifteen minutes, and you will know more than any thread summarising it.

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[removed]215 points·8 months ago

[removed by moderator]

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u/week_four_wall173 points·9 months ago·edited

Push back: an open-label extension tells you about the people who stayed. That is a different question.

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u/draw_up_dizzy58 points·9 months ago

registry entry, protocol, publication — three different documents

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u/arne_ilunga19 points·8 months ago

read the endpoint before you read the headline

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u/aurel_mwangiOP0 points·9 months ago

How long was the randomised phase before any extension?

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u/marit_laurent1 point·8 months ago

Is that intention-to-treat or completers?

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u/line_demir1 point·8 months ago

Yes — the interval is the finding. A point estimate with a wide interval is a hypothesis in a nice font.

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u/sofia_wikstrom101 points·8 months ago

That is a relative risk reduction. Quoting it without the absolute numbers overstates the case considerably.

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