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NCT03430778 Clinical Trial

Effect of Pneumoperitoneum on the Continuous and Non-invasive Hemoglobin Monitoring

Gastric Cancer Clinical Trial

Official title:
Effect of Pneumoperitoneum on the Continuous and Non-invasive Hemoglobin Monitoring for Laparoscopic Gastrectomy: a Randomized Controlled Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03430778
Other study ID # AJIRB-MED-OBS-17-339
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date May 13, 2019

Study information
Verified date May 2019
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of this study is to investigate the effect of pneumoperitoneum on the continuous and non-invasive hemoglobin monitoring during laparoscopic gastrectomy

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date May 13, 2019
Est. primary completion date May 13, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 85 Years
Eligibility Inclusion Criteria:

- Laparoscopic gastrectomy under general anesthesia

Exclusion Criteria:

- atypical hemoglobin disease, infective state, cardiovascular disease, peripheral vascular disease

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• High end-tidal CO2
maintaining of end-tidal CO2 with the range of 40-45 mmHg
• Low CO2 group
maintaining of end-tidal CO2 with the range of 30-35 mmHg

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine Suwon Seoum

Sponsors (1)
Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary difference between SpHb value and SaHb value (SpHb - SaHb) SpHb value is measured by co-oxymetry, and SaHb value is measured by blood sampling. from the start of anesthesia to the end of anesthesia, an average 2 hours
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