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Volume-challenge in Morbid Obesity

Morbid Obesity and Optimization of Preoperative Fluid Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01748513
Enrollment
34
Registered
2012-12-12
Start date
2011-03-31
Completion date
2013-04-30
Last updated
2013-04-30

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

Conditions

Anomaly; Venous Return

Keywords

morbidly obese patients,, preoperative volume-challenge,, transthoracic echocardiography,, TTE,, rapid weight loss,, venous return,, bariatric surgery,, left ventricular outflow tract,, stroke volume,, diastolic function,, hypervolemia,, hypovolemia

Brief summary

Preoperative venous return stability and euvolemia is essential in management of morbidly obese patients. Fluid therapy regimes for patients with high BMI, especially with focus on preoperative management, are rare and not in consensus.The aim of this study was to evaluate preoperative effects of a standardized, ideal body weight (IBW) based volume-challenge on hemodynamics, stroke volume and level of venous return to the heart.

Detailed description

34 morbidly obese patients scheduled for bariatric surgery underwent a preoperative three-week preparation by rapid-weight-loss-diet (RWL) to be accepted for bariatric surgery. Preoperative transthoracic echocardiography (TTE) was performed in the awake state before and after volume-challenge (VC) based on 6ml colloids /kg IBW. Feasibility of standardized VC was evaluated by TTE. Dynamic and non-dynamic echocardiographic indices for VC were studied. Main outcome measures: Volume-responsiveness and level of venous return before and after volume-challenge were assessed by TTE. An increase of stroke volume ≥ 13% was considered as a volume-responder.

Interventions

OTHERpreoperative venous return optimizing

Preoperative transthoracic echocardiography (TTE) was performed in the awake state before and after volume challenge based on 6ml colloids /kg ideal body weight.

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* enrolled for bariatric surgery * BMI ≥ 40 or ≥ 35kg/m2 with co-morbidities * preoperative three-weeks preparation by rapid-weight-loss-diet and weight loss

Exclusion criteria

* untreated significant hypertension * unstable angina pectoris * significant valve regurgitation or stenosis * known severe pulmonary disease

Design outcomes

Primary

MeasureTime frame
level of venous return0,1 hour

Secondary

MeasureTime frame
Volume-responsiveness0,1 hour

Other

MeasureTime frame
Evaluation of feasibility of dynamic and non-dynamic echocardiographic indices for volume challenge1 hour

Countries

Sweden

Outcome results

None listed

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