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c/trialwatch·posted 2 years ago by u/rina_sobczak

[Discussion] the endpoint advice in here is 3 years out of date

Discussion Well Actually ×2 Slow Clap ×3 Cold Box ×1

Thinking out loud about this: the endpoint advice in here is 3 years out of date.

3 years — those are the numbers, and they are the ones I am willing to defend.

Discontinuation rates are a tolerability result. A trial with a strong efficacy number and heavy discontinuation is telling you two things and people only quote one.

Spent an evening with the appendix tables and found the subgroup detail that the entire thread had been speculating about.

Sceptical readings welcome. The confident ones are the ones I distrust.

3,772 up / 300 down93% upvoted51 commentsid 4od7lq6 Apr 2024

51 comments

12 in this archive, depth 4

best — the order this archive was captured in

u/sten_palacios333 points·2 years ago

Relative risk reduction without the baseline rate is uninterpretable. A large relative reduction on a small absolute risk is a small absolute benefit.

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u/alcohol_aversion91 points·2 years ago

This. Intention-to-treat versus completer analysis routinely moves the headline by several points.

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u/annika_fonseca44 points·2 years ago

How long was the randomised phase before any extension?

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u/trialwatch_theoMOD172 points·2 years ago

Retitled: the original quoted a diabetes endpoint as an obesity result.

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u/nikhil_lindqvist45 points·2 years ago

What did the confidence interval look like?

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u/zaid_roos36 points·2 years 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/renal_outcomes_rnephro-curious193 points·2 years ago

trial populations get support that nobody on this board gets

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u/karl_fischer_kev358 points·2 years ago

intention to treat versus completers changes the number substantially

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u/rina_sobczakOP193 points·2 years ago

What was the comparator?

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u/formulary_fighterappeals50 points·2 years ago·edited

Argued for a week about a result and then read the limitations section, which conceded most of my opponent’s point.

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u/rina_sobczakOP30 points·2 years ago

Which trial, and which arm?

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Clinical trial reading group. New readouts, protocol amendments, endpoint definitions, dropout handling, and the difference between a press release and a publication. Absolute risk reduction and number-needed-to-treat are house dialect here.

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