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NCT04060069 Clinical Trial

Pneumoperitoneum and Trendelenburg Position on Fluid Responsiveness

Fluid Responsiveness Clinical Trial

Official title:
Influence of Pneumoperitoneum and Trendelenburg Position on Fluid Responsiveness Predicted by Pulse Pressure Variation and Stroke Volume Variation During Anaesthesia for Laparoscopic Gynaecological Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04060069
Other study ID # KOU GOKAEK 2016/272
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2016
Est. completion date July 1, 2017

Study information
Verified date August 2019
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The increased intraabdominal pressure and intrathoracic pressure due to pneumoperitoneum negatively affect the cardiovascular system, relatively dynamic parameters may vary due to intraoperative fluid therapy.

Description:

After the general anaesthesia induction and intubation, dynamic parameters such as SVV and PPV were monitored by pulse contour analysis.

Recruitment information / eligibility
Status Completed
Enrollment 45
Est. completion date July 1, 2017
Est. primary completion date June 1, 2017
Accepts healthy volunteers No
Gender Female
Age group 19 Years and older
Eligibility Inclusion Criteria:

- Age>18 years old patients

- Will undergo elective laparoscopic gynecological surgery

- ASA I-II

Exclusion Criteria:

- Obese patients (body mass index> 30 kg.m2)

- Patients who had arrhythmia

- Patients who had cardiac insufficiency.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Ringer Lactate
Fluids

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Kocaeli University

Outcome
Type Measure Description Time frame Safety issue
Primary to evaluate how stroke volume variation (%) affected during the Trendelenburg position and pneumoperitoneum to evaluate reliability of stroke volume variation in evaluating the response to fluid administration up to 10 months
Primary to evaluate how pulse pressure variation (%) affected during the Trendelenburg position and pneumoperitoneum to evaluate reliability of pulse pressure variation in evaluating the response to fluid administration up to 10 months
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