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Fluid Responsiveness in Prone Patients

NCT ID: NCT06254456

Last Updated: 2024-02-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

84 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-03-01

Study Completion Date

2028-07-04

Brief Summary

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To assess fluid responsiveness in prone patient

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Detailed Description

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Conditions

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Fluid Responsiveness

Study Design

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Allocation Method

NA

Intervention Model

SEQUENTIAL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Prone patients

Group Type EXPERIMENTAL

End expiratory occlusion test

Intervention Type DIAGNOSTIC_TEST

Fluid responsiveness test

Interventions

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End expiratory occlusion test

Fluid responsiveness test

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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Tidal volume challenges test

Eligibility Criteria

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Inclusion Criteria

* patients planed to prone position for treatment

Exclusion Criteria

* no consent
* arrhythmia
* pregnancy
* pre existing pneumothorax
* pre existing fluid overload
* cannot insert arterial or central venous catheters
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bhumibol Adulyadej Hospital

OTHER

Sponsor Role lead

Responsible Party

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Thanadate Sirithanasarn

Fellowship Training in Critical Care Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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95/66

Identifier Type: -

Identifier Source: org_study_id

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