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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02993497
Other study ID # 1-2016-0063
Secondary ID
Status Completed
Phase N/A
First received December 8, 2016
Last updated November 9, 2017
Start date February 5, 2017
Est. completion date July 4, 2017

Study information

Verified date November 2017
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In patients undergoing spinal anesthesia, the investigators used an Infra-red camera and a respiratory volume monitor to determine the accuracy of the ventilation rate of the infra red camera by measuring the respiratory rate, ventilation volume, and ventilation volume with respiratory volume monitor.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date July 4, 2017
Est. primary completion date July 4, 2017
Accepts healthy volunteers No
Gender Male
Age group 19 Years and older
Eligibility Inclusion Criteria:

- An adult male who underwent endoscopic prostatectomy resection with regular surgery

- An adult male who underwent endoscopic bladder resection with regular surgery

Exclusion Criteria:

- Presenting alteration in respiratory function detected by functional analysis of lung volume and capacity- pneumonectomy patient, severe ipsilateral destroyed lung patient

- Inability to understand or perform the procedure

- ASA(American Society of Anesthesiologists) class 4,5

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Infrared camera
In patients undergoing spinal anesthesia, the respiratory parameters are measured using an Infrared camera.
RVM(Respiratory Volume Monitor)
In patients undergoing spinal anesthesia, the respiratory parameters are measured using an RVM(Respiratory Volume Monitor).

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary The accuracy of breathing measurements The accuracy of breathing measurements between infrared camera and RVM in patients with spinal anesthesia Intraoperative period about 1 hour
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