Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02803424
Other study ID # 4-2016-0311
Secondary ID
Status Completed
Phase N/A
First received June 9, 2016
Last updated December 25, 2016
Start date June 2016
Est. completion date December 2016

Study information

Verified date December 2016
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The steep trendelenburg position and pneumoperitoneum during laparoscopic surgery have the potential to cause an adverse effects on respiratory mechanics and gas exchange. Autoflow-volume controlled ventilation may improve lung compliance and reduce airway peak pressure. Therefore, the aim of this study is to evaluate whether Autoflow-volume controlled ventilation improves gas exchange and respiratory mechanics in patients undergoing robot-assisted laparoscopic radical prostatectomy.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

1. Adult male patients scheduled for elective robot-assisted laparoscopic radical prostatectomy undergoing general anesthesia

Exclusion Criteria:

1. chronic obstructive respiratory diseases

2. heart failure

3. body mass index (BMI >30 kg/m2)

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)


Related Conditions & MeSH terms

  • Pneumoperitoneum
  • Robot-assisted Laparoscopic Radical Prostatectomy Undergoing General Anesthesia

Intervention

Other:
Volume controlled ventilation
During anesthesia and surgical procedure, volume-controlled ventilation will be applied with an inspiration:expiration ratio of 1:2 and a tidal volume of 8 mL per ideal body weight (kg) without ventilatory mode change.
Autoflow-volume controlled ventilation
After tracheal intubation, volume-controlled ventilation will be initiated with an I:E ratio of 1:2 and a tidal volume of 8 mL per ideal body weight (kg). Immediately after CO2 pneumoperitoneum with steep Trendelenburg positioning, Autoflow-volume controlled ventilation will be applied instead of volume-controlled ventilation. Immediately after CO2 desufflation and supine positioning, volume-controlled ventilation will be applied again.

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Kim MS, Kim NY, Lee KY, Choi YD, Hong JH, Bai SJ. The impact of two different inspiratory to expiratory ratios (1:1 and 1:2) on respiratory mechanics and oxygenation during volume-controlled ventilation in robot-assisted laparoscopic radical prostatectomy: a randomized controlled trial. Can J Anaesth. 2015 Sep;62(9):979-87. doi: 10.1007/s12630-015-0383-2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary arterial oxygen tension (PaO2) Arterial oxygen tension (PaO2) obtained from arterial blood gas analysis 30 minutes after steep trendelenburg position and pneumoperitoneum. No
Secondary The peak inspiratory pressure The peak inspiratory pressure during mechanical ventilation with endotracheal intubation under general anesthesia 10 minutes after anesthesia induction, 30 and 60 minutes after steep trendelenburg position and pneumoperitoneum, and 10 minutes after supine position and CO2 desufflation. No