Echocardiography Examination Of The Cardiac Effects Of Different Regional Anesthesia Methods

NCT ID: NCT04975386

Last Updated: 2021-07-29

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

62 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-07-29

Study Completion Date

2022-08-15

Brief Summary

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Nerve blocks applied with neuraxial anesthesia and ultrasonography are used for many operations today. Neuraxial blocks cause varying degrees of decrease in the blood pressure level of the patients. Peripheral blocks may be preferred to avoid the cardiac effects of the neuraxial anesthesia method.

Detailed Description

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The hypothesis of this study was that spinal anesthesia applied in intertrochanteric femoral fracture operations caused hypotension by lowering the cardiac ejection fraction.

In our study, The investigators aimed to find out the effect of different regional anesthesia methods on the cardiac function of the patients by echocardiography.

Conditions

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Femur Fracture Spinal Anesthesia Lumbar Plexus Block

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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spinal anesthesia

Group Type ACTIVE_COMPARATOR

Transthoracic echocardiogram

Intervention Type DEVICE

Transthoracic echocardiogram will be performed before the operation and at certain time intervals during the operation.

lumbar plexus+sacral plexus block

Group Type ACTIVE_COMPARATOR

Transthoracic echocardiogram

Intervention Type DEVICE

Transthoracic echocardiogram will be performed before the operation and at certain time intervals during the operation.

Interventions

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Transthoracic echocardiogram

Transthoracic echocardiogram will be performed before the operation and at certain time intervals during the operation.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 60-100 years old
* American Society of Anesthesiologist Score I-IV

Exclusion Criteria

* Local anesthetic allergy
* Bleeding disorder
* Mental disorder
* Allergy to drugs used
* Body mass index above 30
Minimum Eligible Age

60 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bursa Yuksek Ihtisas Training and Research Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Korgün Ökmen

Principal Investigator ,Assoc. PhD. M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Durdu M.D Kahraman Yıldız

Role: PRINCIPAL_INVESTIGATOR

Bursa Yuksek Ihtisas Training and Research Hospital

Central Contacts

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Korgün Ökmen, Assoc. PhD.

Role: CONTACT

+905057081021

Korgün M.D Ökmen, Assoc. PhD.

Role: CONTACT

+905057081021

Other Identifiers

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2011-KAEK-25 2020/10-03

Identifier Type: -

Identifier Source: org_study_id

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