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What Should be the Anesthesia Method in Endobronchial Coil Treatment

Comparison of General Anesthesia and Deep Sedation in Enbronchial Coil Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03652324
Enrollment
32
Registered
2018-08-29
Start date
2018-03-28
Completion date
2018-08-28
Last updated
2018-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coil Treatment, Deep Sedation

Keywords

coil treatment, general anesthesia, deep sedation

Brief summary

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.

Interventions

OTHERmethod

to compare the use of general anesthesia and deep sedation

Sponsors

Bozok University
CollaboratorOTHER
TC Erciyes University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients diagnosed with COPD with undergoing BLVR coil treatment.

Exclusion criteria

* patients who refuse to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
recovery time measurement2 hoursto compare the recovery time in both groups
complication rate2 hoursto compare the complication rate in both groups

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026