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NCT05574400 · ClinicalTrials.gov registry record · Phase 2

The Caffeine, Postoperative Delirium, and Change in Outcomes After Surgery (CAPACHINOS-2) Study

A Phase 2 study of Mild Cognitive Impairment and Postoperative Delirium, sponsored by University of Michigan.

Recruiting
Registry status
Phase 2
Development phase
250
Enrollment target
1
Study location

NCT05574400: Recruiting Phase 2 study of Mild Cognitive Impairment and Postoperative Delirium, sponsored by University of Michigan.

NCT05574400 is a Phase 2 study of Mild Cognitive Impairment and Postoperative Delirium that is actively recruiting participants, run by University of Michigan. The registered enrollment target is 250 participants, below the 1,269-participant average among 205 other Mild Cognitive Impairment trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05574400, a Phase 2 study of Mild Cognitive Impairment and Postoperative Delirium, is actively recruiting participants, sponsored by University of Michigan.

RECRUITING
Registry status
Phase 2
Development phase
250 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to test the effects of caffeine on neurocognitive and clinical recovery after major surgery. Specifically, this trial tests the primary hypothesis that caffeine will reduce the incidence of postoperative delirium.

Primary Outcome

Any positive delirium screen (yes/no) as determined by the long-form Confusion Assessment Method (CAM), and supplemented by a validated daily chart review method.

Interventions

  • DRUG Dextrose Water
  • DRUG Caffeine citrate

Study Locations (1)

Michigan

  • Michigan Medicine - Ann Arbor

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2023-02-20
Est. Completion 2026-05-31
Phase Phase 2
University of Michigan

1,327 total trials

What NCT05574400 shows while recruiting

NCT05574400 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 1,269-participant average among 205 other Mild Cognitive Impairment trials with a reported enrollment target (80% lower).

The record links to 3 conditions, with Mild Cognitive Impairment appearing as the primary indexed condition, and to 2 interventions - of which Dextrose Water is the first listed.

NCT05574400 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT05574400 about?

NCT05574400 is a clinical study titled "The Caffeine, Postoperative Delirium, and Change in Outcomes After Surgery (CAPACHINOS-2) Study". The objective of this study is to test the effects of caffeine on neurocognitive and clinical recovery after major surgery. Specifically, this trial tests the primary hypothesis that caffeine will reduce the incidence of postoperative delirium.

What is the current status of trial NCT05574400?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 250 participants. The study started on 2023-02-20. Estimated completion is 2026-05-31.

What conditions does trial NCT05574400 study?

This clinical trial studies the following conditions: Mild Cognitive Impairment, Postoperative Delirium, Postoperative Cognitive Dysfunction.

What interventions are being tested in trial NCT05574400?

The interventions under investigation include: Dextrose Water (DRUG), Caffeine citrate (DRUG).

Who is sponsoring clinical trial NCT05574400?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05574400 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Mild Cognitive Impairment

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05574400's enrollment target sits among peer trials

250 35th of 205 higher than 170 of 205 other Mild Cognitive Impairment trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Mild Cognitive Impairment trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05574400, the US trial registry maintained by the National Library of Medicine. NCT05574400 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.