Clinical trials: Volume
Buttocks Volume Loss
Clinical Study for the Evaluation of the Effectiveness of Use of a Poly-L Lactic Acid Injectable Filler for the Aesthetic Treatment of Buttocks Volume Depression
The purpose of this study is to assess the effectiveness and safety of Gana X, a Poly L-lactic acid filler for the aesthetic treatment of buttocks.
- Trial name
- PLLA (NCT05363163)
- Testing
- Gana X
- Where
- France
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- GCS Co., Ltd
Gastric Volume, Breast Cancer Female
Effect of Positive End-expiratory Pressure on the Gastric Volume
The main purpose of this study is to quantitatively evaluate the effect of applying PEEP during the use of SGA on gastric volume, aiming to provide objective evidence regarding the potential side effects, such as gastric volume…
- Conditions
- Gastric Volume, Breast Cancer Female, Anesthesia Complication
- Trial name
- NCT06861569
- Testing
- Positive end expiratory pressure
- Volunteers
- 128 people
- Sponsor
- Seoul National University Bundang Hospital
Hyponatremia With Excess Extracellular Fluid Volume, Cirrhosis, Liver
Albumin for Management of Hypervolemic Hyponatremia (AlbuCAT)
resolution of hyponatremia, defined as an increase in serum sodium of more than 5 mEq/L with a final value > 130 mEq/L, maintained for at least 48 consecutive hours during the 10-day treatment period
- Trial name
- AlbuCAT (NCT03941405)
- Testing
- Albumin treatment
- Where
- 3 sites in Spain
- Volunteers
- 52 people
- Sponsor
- Fundacion Clinic per a la Recerca Biomédica
Spinal Induced Hypotension, Geriatric Population
Spinal-Induced Hypotension in Geriatric Patients
The study will be conducted to asses preoperative condition of venous system by VExUS score and it's relation with the incidence of spinal induced hypotension in geriatric patients undergoing surgery with spinal anaesthesia.
- Conditions
- Spinal Induced Hypotension, Geriatric Population, Intravascular Volume
- Trial name
- NCT05862298
- Testing
- venous excess ultrasound score
- Where
- Egypt
- Volunteers
- 120 people
- Sponsor
- Tanta University
Bladder Disease, Bladder Retention Volume
ECHO-012 Kosmos Bladder Clinical Validation Study
The goal of this clinical trial is to compare the Kosmos Automatic Bladder Volume to the manual annotated bladder volume in participants across gender (male and female), age (children ages 7-17 and adults 18-89), and BMI strata…
- Conditions
- Bladder Disease, Bladder Retention Volume, Bladder Dysfunction, Bladder Function
- Trial name
- NCT06792851
- Testing
- Kosmos Bladder Volume Algorithm
- Where
- United States
- Volunteers
- 146 people, healthy volunteers welcome
- Sponsor
- EchoNous Inc.
Gastric Volume
Ultrasound Assessment of Metoclopramide's Effect on Stomach Volume in Urgent Pediatric Trauma Surgery
assess the efficacy of metoclopramide in reducing the gastric contents and volume in pediatric trauma prepared for urgent surgical interventions.
- Trial name
- NCT06793267
- Testing
- Metoclopramide (Maxolon), Saline
- Volunteers
- 70 people
- Sponsor
- Assiut University
Gastric Residual Volume
Effect of Metoclopramide Versus Erythromycin on on Gastric Residual Volume
In emergencies, it may be necessary to anaesthetize who are not fully starved and consequently at risk of pulmonary aspiration. Pregnancy are recognized to be at increased risk of aspiration compared with non-pregnancy.
- Trial name
- NCT04682691
- Testing
- Erythromycin (400mg), metoclopramide (10mg), naturally flavored water
- Where
- Egypt
- Volunteers
- 50 people
- Sponsor
- Cairo University
Cardiopulmonary Failure, Myocardial Infarction (MI)
COR-INSIGHT: Optimizing Cardiovascular and Cardiopulmonary Outcomes with AI-Driven Multiplexed Indications Using COR ECG Wearable
The COR-INSIGHT trial aims to evaluate the effectiveness of Peerbridge COR advanced ambulatory ECG wearables (COR 1.0 and COR 2.0) in accurately and non-invasively detecting cardiovascular and cardiopulmonary conditions using…
- Conditions
- Cardiopulmonary Failure, Myocardial Infarction (MI), Heart Decompensation, Heart Failure
- Trial name
- COR-INSIGHT (NCT06763549)
- Testing
- SUBPROTOCOL A, SUBPROTOCOL B, SUBPROTOCOL C
- Where
- United States
- Volunteers
- 15,000 people, healthy volunteers welcome
- Sponsor
- Peerbridge Health, Inc
Midface Volume Deficit
Sculptra for Correction of Midface Volume Deficit and/or Midface Contour Deficiency
This is a randomized, evaluator-blinded, no-treatment controlled study in participants with Midface Volume Deficit and/or Midface Contour Deficiency.
- Trial name
- NCT04132518
- Testing
- Sculptra
- Where
- 6 sites in China
- Volunteers
- 205 people
- Sponsor
- Galderma R&D
Midface Volume Deficit
To Evaluate the Performance and Safety of YVOIRE Volume Plus for Improvement of Mid-face Volume
A Study to Evaluate the Performance and Safety of YVOIRE volume plus for Temporary Improvement of Mid-face Volume
- Trial name
- NCT04784299
- Testing
- YVOIRE volume plus, Restylane Lyft with Lidocaine
- Where
- Germany
- Volunteers
- 105 people, healthy volunteers welcome
- Sponsor
- LG Chem
Pulse Pressure Variation, Stroke Volume Variation
Peripheral Venous Pressure Variation, Pulse Pressure Variation and Pleth Variability Index for Fluid Responsiveness
Pulse pressure variation (PPV) and pleth variability index (PVI) are widely used in clinical practice as indicators of the responsiveness to fluid therapy in patients receiving mechanical ventilation.
- Conditions
- Pulse Pressure Variation, Stroke Volume Variation, Pleth Variability Index
- Trial name
- NCT06733389
- Testing
- peripheral waveform collection
- Where
- South Korea
- Volunteers
- 150 people
- Sponsor
- Seoul National University Bundang Hospital
Peripheral Vein, Arterial Wave Reflections
Deep Learning Model for Predicting a Peripheral Venous Waveform-based Pulse Pressure Variation
Pulse pressure variation is a monitoring index that indicates the response to fluid therapy in patients receiving mechanical ventilation, and is used as a reference for patients with unstable hemodynamic conditions.
- Conditions
- Peripheral Vein, Arterial Wave Reflections, Pulse Pressure Variation, Stroke Volume Variation
- Trial name
- NCT06734650
- Testing
- peripheral waveform collection
- Where
- South Korea
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- Seoul National University Bundang Hospital
Mid Face Volume Deficit
THIODERM STRONG Compared to Juvéderm® VOLUMA® Lidocaine for the Treatment of Midface Volume Deficit
This mono-center clinical investigation is intended to evaluate the safety and effectiveness of THIODERM STRONG (test device) in the correction of moderate to severe midface volume deficit compared to Juvéderm® VOLUMA® Lidocaine…
- Trial name
- TIMI (NCT06128109)
- Testing
- Thioderm Strong, Juvéderm VOLUMA Lidocaine
- Where
- Austria
- Volunteers
- 20 people
- Sponsor
- Croma-Pharma GmbH
Midface Volume Deficit
A 52-week Clinical Investigation of Princess® VOLUME PLUS Lidocaine in Subjects With Midface Volume Deficit
This investigation aims to confirm the safety and effectiveness of Princess VOLUME PLUS Lidocaine in midface volume deficit augmentation and includes a long term safety followup.
- Trial name
- PRIMAvera (NCT03532126)
- Testing
- Dermal filler for midface deficit
- Where
- 4 sites in Austria, Germany
- Volunteers
- 91 people
- Sponsor
- Croma-Pharma GmbH
The Relationship Between TAPSE Value and Volume
Relationship of Preoperative Fasting With Tricuspid Annular Plane Systolic Excursion
The aim of our study is to try to establish a relationship between preoperative fasting-related volume changes and tricuspid annular plane systolic excursion (TAPSE), and to determine whether there are changes in right…
- Trial name
- (TAPSE) (NCT06105866)
- Testing
- Tricuspid Annular Plane Systolic Excursion
- Where
- Turkey (Türkiye)
- Volunteers
- 100 people
- Sponsor
- Aydin Adnan Menderes University
Gastric Residual Volume
Ultrasound Vs. Free Drainage for Gastric Volume in ICU Patients on Enteral Nutrition
This study aims to evaluate the compatibility of gastric volume (GV) measurements obtained through ultrasound with the free drainage method in intensive care patients receiving enteral nutrition under three different protocols.
- Trial name
- NCT06700759
- Where
- Turkey (Türkiye)
- Volunteers
- 78 people
- Sponsor
- Ilkay Ceylan
Nasolabial Folds, Mid Face Volume Loss
Evaluate the Post-marketing Efficacy and Safety of Eptq S and Eptq Lidocaine S
This study in multi-center, prospective and observational study. The purpose of this study is to observe effects and safety of hyaluronic acid filler series, eptq S and eptq Lidocaine S, for facial volume and folds.
- Conditions
- Nasolabial Folds, Mid Face Volume Loss, Lip Volume Enhancement
- Trial name
- NCT06699147
- Testing
- Hyaluronic Acid (HA)
- Where
- South Korea
- Volunteers
- 238 people
- Sponsor
- Jetema Co., Ltd.
Volume Assessment, Gummy Smile
Assessment of The Accuracy of Complete Crown 3D Superimposition Technique Relative to The Gold Standard Technique for Digital Quantification of Volumetric Soft Tissue Changes in The Esthetic Zone
The aim of this study is to assess the precision of the complete crown technique employed for the superimposition of 3D models, specifically in the quantitative volumetric evaluation of gingival tissues.
- Trial name
- NCT06673576
- Testing
- Complete crown technique for superimposition, Gold standard technique for superimposition
- Where
- Egypt
- Volunteers
- 12 people, healthy volunteers welcome
- Sponsor
- British University In Egypt
Perioperative Volume Replacement, Hydroxyethyl Starch
Safety and Efficacy of Perioperative Volume Replacement with Volulyte 6% in Moderate-to-high Cardiovascular Risk Patients Having Major Abdominal Surgery
The investigators propose a multicenter randomized trial to test the renal safety of 6% hydroxyethyl starch (HES) 130/0.4 combined with sodium acetate Ringer's crystalloid solution in moderate-to-high cardiovascular risk patients…
- Trial name
- NCT06663254
- Testing
- Hydroxyethyl starch 130/0.4, Sodium acetate Ringer
- Where
- 6 sites in China
- Volunteers
- 410 people
- Sponsor
- Xiangya Hospital of Central South University
Acute Decompensated Heart Failure, Volume Overload
Acetazolamide in Decompensated Heart Failure With Volume OveRload (ADVOR)
This clinical research study is being conducted in multiple hospitals in Belgium and approximately 519 patients with acute decompensated heart failure are expected to participate.
- Trial name
- Advor (NCT03505788)
- Testing
- Acetazolamide
- Where
- Belgium
- Volunteers
- 519 people
- Sponsor
- Ziekenhuis Oost-Limburg