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NCT06129188 · ClinicalTrials.gov registry record · Phase 1
Comparison of Procedural Sedation in TEE
A Phase 1 study of Anesthesia, sponsored by University of Alabama at Birmingham.
- Completed
- Registry status
- Phase 1
- Development phase
- 105
- Enrollment target
- 1
- Study location
NCT06129188 is a Phase 1 study of Anesthesia that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 105 participants, below the 109,408-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06129188, a Phase 1 study of Anesthesia, has completed, sponsored by University of Alabama at Birmingham.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 105 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this proposal is to conduct a prospective randomized study comparing the utility of sedating patients undergoing transesophageal echocardiographic studies with a novel, recently-FDA-approved sedative agent, remimazolam, versus the sedative used in our current practice at UAB, propofol. This study will investigate whether remimazolam offers any benefit over current care vis-à-vis hemodynamics or efficiency/throughput. This study will be conducted at the University of Alabama at Birmingham. All outpatients and inpatients scheduled for elective/non-emergent TEE in the UAB Heart and Vascular Center TEE lab will be considered for enrollment.
Conditions Studied
Interventions
- DRUG Remimazolam
- DRUG Propofol
Study Locations (1)
Alabama
- University of Alabama at Birmingham Hospital - Birmingham
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 105 participants |
| Start Date | 2025-02-25 |
| Est. Completion | 2025-12-01 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06129188
The ClinicalTrials.gov registry entry for NCT06129188 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 109,408-participant average among 57 other Anesthesia trials with a reported enrollment target (100% lower). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Anesthesia appearing as the primary indexed condition, and to 2 interventions - of which Remimazolam is the first listed.
NCT06129188 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.
Frequently Asked Questions
What is clinical trial NCT06129188 about?
NCT06129188 is a clinical study titled "Comparison of Procedural Sedation in TEE". The objective of this proposal is to conduct a prospective randomized study comparing the utility of sedating patients undergoing transesophageal echocardiographic studies with a novel, recently-FDA-approved sedative agent, remimazolam, versus the sedative used in our current practice at UAB, propof...
What is the current status of trial NCT06129188?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 105 participants. The study started on 2025-02-25. Estimated completion is 2025-12-01.
What conditions does trial NCT06129188 study?
This clinical trial studies the following conditions: Anesthesia.
What interventions are being tested in trial NCT06129188?
The interventions under investigation include: Remimazolam (DRUG), Propofol (DRUG).
Who is sponsoring clinical trial NCT06129188?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06129188 being conducted?
This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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