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NCT06533111 · ClinicalTrials.gov registry record · NA
Improving Surgical Patient Outcomes Through Implementation of a SemiStructured Intraoperative Anesthesia Handoff Tool
A NA study of Postoperative Complications, sponsored by The University of Texas Health Science Center, Houston.
- Recruiting
- Registry status
- NA
- Development phase
- 4,500
- Enrollment target
- 1
- Study location
NCT06533111: Recruiting NA study of Postoperative Complications, sponsored by The University of Texas Health Science Center, Houston.
NCT06533111 is a NA study of Postoperative Complications that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 4,500 participants, above the 337-participant average among 20 other Postoperative Complications trials with a reported enrollment target (1235% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06533111, a NA study of Postoperative Complications, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.
- RECRUITING
- Registry status
- NA
- Development phase
- 4,500 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess the impact of a semi-structured intraoperative anesthesia handoff tool on patient outcomes and to assess the validity of the 5-Factor Perceived Shared Mental Model Scale (5-PSMMS) in a healthcare setting and whether the perception of Shared Mental Model (SMM) mediates the effect of the intraoperative handoff tool on postoperative outcomes
Conditions Studied
Interventions
- OTHER Usual care
- OTHER Epic Health Record semi-structured handoff cognitive aid
Study Locations (1)
Texas
- The University of Texas Health Science Center at Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4,500 participants |
| Start Date | 2024-11-01 |
| Est. Completion | 2026-05-31 |
| Phase | NA |
What NCT06533111 shows while recruiting
NCT06533111 is an interventional study that assigns participants to a tested intervention. Its 4,500 participants enrollment target places it among the larger protocols in the corpus, above the 337-participant average among 20 other Postoperative Complications trials with a reported enrollment target (1235% higher).
The record links to 1 condition, with Postoperative Complications appearing as the primary indexed condition, and to 2 interventions - of which Usual care is the first listed.
NCT06533111 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT06533111 about?
NCT06533111 is a clinical study titled "Improving Surgical Patient Outcomes Through Implementation of a SemiStructured Intraoperative Anesthesia Handoff Tool". The purpose of this study is to assess the impact of a semi-structured intraoperative anesthesia handoff tool on patient outcomes and to assess the validity of the 5-Factor Perceived Shared Mental Model Scale (5-PSMMS) in a healthcare setting and whether the perception of Shared Mental Model (SMM) m...
What is the current status of trial NCT06533111?
This trial is currently recruiting. It is a NA study. The enrollment target is 4,500 participants. The study started on 2024-11-01. Estimated completion is 2026-05-31.
What conditions does trial NCT06533111 study?
This clinical trial studies the following conditions: Postoperative Complications.
What interventions are being tested in trial NCT06533111?
The interventions under investigation include: Usual care (OTHER), Epic Health Record semi-structured handoff cognitive aid (OTHER).
Who is sponsoring clinical trial NCT06533111?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06533111 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Complications
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 NCT06533111's enrollment target sits among peer trials
4,500 1st of 20 higher than 20 of 20 other Postoperative Complications trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Complications 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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