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What Should be the Anesthesia Method in Endobronchial Coil Treatment

NCT ID: NCT03652324

Last Updated: 2018-08-31

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

COMPLETED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-28

Study Completion Date

2018-08-28

Brief Summary

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This prospective, randomize study was conducted in a university hospital. Bronchoscopic lung volume reduction (BLVR) coil treatment has recently been introduced into clinical practice as an alternative for patients chronic obstructive pulmonary disease (COPD) with severe refractory heterorogenous emphysema to conventional medical treatment. Thirty two patients diagnosed with (COPD) with severe refractory heterorogenous emphysema undergoing BLVR coil treatment were included in the study. Seventeen procedure were performed under general anesthesia and fifteen procedure were performed under deep sedation-analgesia. in the general anesthesia group peak pressure, air leakage and end-tidal carbon dioxide were recorded. In the both groups pulse oximeter, transcutaneous carbondioxide, recovery time, bronchospasm, laryngospasm, pneumothorax, massive bleeding were recorded.

Detailed Description

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Conditions

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Coil Treatment Deep Sedation

Keywords

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coil treatment general anesthesia deep sedation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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randomized

Group Type OTHER

method

Intervention Type OTHER

to compare the use of general anesthesia and deep sedation

Interventions

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method

to compare the use of general anesthesia and deep sedation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients diagnosed with COPD with undergoing BLVR coil treatment.

Exclusion Criteria

* patients who refuse to participate in the study
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bozok University

OTHER

Sponsor Role collaborator

TC Erciyes University

OTHER

Sponsor Role lead

Responsible Party

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Gamze Talih

Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Bozok University

Yozgat, Eyalet/Yerleşke, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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60174989-23

Identifier Type: -

Identifier Source: org_study_id