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Impact of Size of Gastric Sleeve on the Weight Loss. Correlation With Gastric Function and Endocrine-metabolic Changes.

Primary Purpose

Obesity, Morbid

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Bougie Size 33 Fr
Bougie Size 42 Fr
Distance pylorus 2 cm
Distance pylorus 5 cm
Sponsored by
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity, Morbid focused on measuring Surgery, Morbid Obesity, Bariatric surgery, Sleeve gastrectomy, Bougie Size, Distance from pylorus, Hormones, Gastric remanent

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age more than 18 years and less than 65 years
  • BMI more than 40 kg/m2 or more than 35 kg/m2 with comorbidities likely to improve after weight loss.
  • Morbid obesity established at least five years.
  • Continued failures to adequately supervised conservative treatments
  • Absence of endocrine disorders that are due to morbid obesity.
  • Psychological stability:

    • No alcohol or drug abuse.
    • Absence of major psychiatric disorders (schizophrenia, psychosis), mental retardation, eating disorders (bulimia nervosa).
  • Ability to understand the mechanisms to lose weight with surgery and understand that not always achieved good results.
  • Understand that the goal of surgery is to achieve the ideal weight.
  • Commitment for Adherence to surveillance guidelines after surgery
  • Informed consent after receiving all the necessary information (oral and written).
  • Women of childbearing age should avoid pregnancy for at least the first year after surgery

Exclusion Criteria:

  • No acceptance
  • Age less than 18 years or more than 65 years
  • Previous bariatric surgery
  • Previous gastric surgery
  • Inflammatory bowel disease

Sites / Locations

  • Hospital de la Santa Creu i Sant PauRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Bougie Size 33Fr Distance pylorus 2 cm

Bougie Size 33Fr Distance pylorus 5 cm

Bougie Size 42Fr Distance pylorus 2 cm

Bougie Size 42Fr Distance pylorus 5 cm

Arm Description

Sleeve gastrectomy with a 33Fr bougie size and 2 cm distance from the pylorus.

Sleeve gastrectomy with a 33Fr bougie size and 5 cm distance from the pylorus

Sleeve gastrectomy with a 42Fr bougie size and 2 cm distance from the pylorus

Sleeve gastrectomy with a 42Fr bougie size and 2 cm distance from the pylorus

Outcomes

Primary Outcome Measures

Body mass index
Gastric volume

Secondary Outcome Measures

Gastric emptying time
Lower esophageal sphincter pressure
Number of gastroesophageal reflux episodes

Full Information

First Posted
November 19, 2013
Last Updated
September 29, 2015
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
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1. Study Identification

Unique Protocol Identification Number
NCT02144545
Brief Title
Impact of Size of Gastric Sleeve on the Weight Loss. Correlation With Gastric Function and Endocrine-metabolic Changes.
Official Title
Study of Impact of the Size of Gastric Sleeve o the Weight Loss in Patients Submitted to Bariatric Surgery. Evaluation of Changes in Gastric Motility and Endocrine-metabolic Function.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Unknown status
Study Start Date
October 2013 (undefined)
Primary Completion Date
October 2016 (Anticipated)
Study Completion Date
October 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Morbid Obesity (MO) is considered the most important epidemic in the developed world in the twenty-first century. After initial assessment of morbidly obese patients and the exclusion of potentially correctable causes, management involves a combination of dietary changes, cognitive therapy, physical activity, psychological support and pharmacological treatment. However, any combination of these factors has proven long-term effectiveness in achieving significant and sustained reduction of excess weight. Currently, surgery is the only treatment capable of achieving this goal, interacting also with significant improvement in quality of life and overall long-term mortality. In recent years, several authors have reported excellent short-term results with performing sleeve gastrectomy, but whether some aspects regarding the variability of gastric tubulization design could influence the results obtained in relation to weight loss and functional changes and gastric hormones. The main objective of this study is to assess the size of the gastric tubulization (based probe calibration and the distance from the pylorus to which initiate gastric section) that can provide a better clinical outcome (such as excess weight loss) in patients undergoing surgery for morbid obesity. Secondary objectives were to assess the morphological changes, physiological and hormonal obtained according to the size of the gastric tubulization and its effect on weight loss patients.
Detailed Description
HYPOTHESIS Surgical major factors which determine the size of the gastric pouch after performing a a sleeve gastrectomy are the diameter of the remanent stomach (influenced by the diameter of the bougie size) and the residual antrum. Whereas gastrectomy is a restrictive procedure, we postulate that the variation of these factors can have a significant impact on clinical outcomes in terms of weight loss and improvement in comorbidities in addition to possible changes in the hormone pattern OBJECTIVE: Primary Outcome Measure: Weight loss one year after surgery Secondary Outcome Measures: Morphological changes induced by the size of the gastric tubulization Gastric antrum volume Gastric body volume Correlation between gastric volumes and weight loss Gastric emptying Hormone levels (before and after surgery) and relation with weight loss Quality of life DATA TO ANALIZE We will analyze the following key variables: BMI (body mass index) Preoperative gastric volume Postoperative gastric volume. An evaluation of the variation of these data in two stages (one month and one year after surgery) in each patient group and the comparison will be made between groups. Secondary variables to analyze are: - Gastric emptying, analyzed in relation to baseline (preoperative) Lower esophageal sphincter pressure The number of episodes of gastroesophageal reflux, the number of reflux episodes longer than 5 minutes, the percentage of time with pH below 4 Plasma hormones listed below An evaluation of the temporary modification of these variables to the month and year of surgery in relation to preoperative values in each patient group and the comparison will be made between the four groups. Gastric volume study Methodology For the evaluation of the patients an abdominal CT scan in multislice device will be performed. Diluted oral contrast was administered 3% (amidotrizoate meglumine, sodium amidotrizoate Gastrografin ®) for a maximum distension of the stomach or gastric remnant in order to assess gastric volume or its remnant. Cuts will be made within 45 minutes of ingestion of oral contrast and perform a CT without intravenous contrast supine, including from the tracheal carina to pubic symphysis. Cuts are initiated above the diaphragmatic hiatus to the carina level, in order to evaluate possible migration flows of the gastric remnant as reported in recent publications in this type of surgery. All cases must be supervised by a radiologist as part of the study team to validate the images obtained with the purpose of being of the highest quality 3D for further processing. Validate the optimal degree of gastric distension. The data collected and stored in DICOM format for further manipulation 3D. The study protocol provides for the realization of three CT scans: Preoperative CT Be assessed the maximum gastric volume and the height of the esophagogastric junction in order to quantify the possible migration. CT one month after surgery Possible to quantify the volume of gastric remnant and assess whether it has increased in volume. This data would adjust the actual volume of the remnant and apply it to the 3D model. Assess whether there is cranial migration of esophagogastric junction and gastric any late postoperative complications. Will correlate with weight loss. CT one year after surgery Rating final state of the stomach, final quantification of the residual volume and correlation with final weight loss. Final assessment of the possible complications and gastric migration. Scintigraphic evaluation Methodology Patient preparation It is important for the patient a 12 hours fast, to ensure that the stomach is empty. In addition, the patient may not smoke or take medication that could interfere with gastric motility. In diabetic patients, the CT scan wil be performed first thing in the morning, after the injection of insulin. Radiopharmaceutical To get the most information in a single tracer, it is best to mark the solid component. With solids, in addition to assessing antral motility is measured indirectly by the state of the gastric tone, once they have been crushed and can be emptied. For this, 50 g huevina will beat with 1 mCi (37 MBq) of 99m Tc-sulfur colloid and immediately cook a tortilla. Gamma camera Dual-head with low-energy collimator and medium resolution (LEAP) Procedure Immediately after ingesting the food (in less than 10 minutes), it will proceed to detect of the stomach with the patient standing. Among the various detections, the patient should remain seated. Will immediately perform a baseline image and subsequently post-ingestion, anterior and posterior views of 2 minutes duration every 15 minutes for two hours. Processed ROI is drawn over the gastric area, except in the first image to be included in all activity, even if there is intestinal. The software determines gastric accounts every time and projection (anterior and posterior) and geometric mean (Qty * Cpost). Also determined for each point the residual percentage compared to the initial activity. Time There will be temporary in the same sequence as in the radiological evaluation: preoperative and postoperative assessment at one month and a year Functional esophagogastric evaluation Methodology Esophageal manometry and pH monitoring will be performed in all patients included in the study . The tests were carried out in the Digestive Pathology Service from Hospital Santa Creu i Sant Pau. Esophageal manometry catheter is made with a polyvinyl four holes spaced 5 inches between them. The distal end is connected to an external pressure transducer and the electrical signal is processed and analyzed by the computer program (PC Polygraf , Synectics Medical). It takes eight hours prior fasting , previously suspending medication that may alter esophageal motility and modifying stomach acid secretion. The catheter is inserted through the mouth into four channels that have reached the stomach. Recording the intra- gastric pressure at the end of expiration and is used as reference. The manometric evaluation of the lower esophageal sphincter is performed by a slow withdrawal. Record the resting pressure, length, location relative to the nasal ala and relaxation post swallow . Esophageal motor activity (amplitude and duration of the waves, peristaltic waves percentage of simultaneous post swallow), is evaluated by slowly withdrawn after conducting at least 10 swallows 3-5 cc of water every 20 seconds. Finally, we evaluate the upper esophageal sphincter activity. Pharyngeal pressure is recorded, the resting pressure of the upper esophageal sphincter pharyngo - esophageal coordination and upper esophageal sphincter relaxation after dry or liquid swallows every 20 seconds. After esophageal manometry pH monitoring is performed . Using a single-use probe 2 channels. We introduce the probe pH monitoring through the nose to reach the lower esophageal sphincter ( by reference to the location of the lower esophageal sphincter by manometry found). Probe is then removed, leaving 5 cm above the lower esophageal sphincter . The patient is instructed to perform their usual daily activity, a symptom diary recording . The probe is connected to a Holter apparatus that recorded during 24 the number of reflows , measure their duration in minutes and the duration of the longest reflux episode, the percentage of time that esophageal pH is less than 4. All measurements were recorded at both the proximal and distal esophagus. After 24 hours the tube is removed and information is processed by a computer program (PC Polygraf, Synectics Medical). Time The evaluation was conducted in three stages: pre-and postoperative assessment (within 2 days, 3 months and one year). - Hormonal and glucose metabolism It will carry out the following hormonal determinations: • Insulin • Glucagon • GLP-1 • GIP • Ghrelin • Leptin • Adiponectin Peptide YY Methodology Blood samples were made a week before surgery (in the Day Hospital of Endocrinology), during admission in ward General Surgery (on the 2nd postoperative day) and at 3 months and one year after surgery (in the Day Hospital of Endocrinology). To this end, each patient was placed in a peripheral vein upper extremity. The first draw will be fasting. Ten minutes later, given a standard meal and proceed to the extraction of blood samples at the following times: the end of the intake postprandial samples (at 20, 60 and 120 respectively). Times: The determinations were carried out: one week before surgery postoperative day 2 a year

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Morbid
Keywords
Surgery, Morbid Obesity, Bariatric surgery, Sleeve gastrectomy, Bougie Size, Distance from pylorus, Hormones, Gastric remanent

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bougie Size 33Fr Distance pylorus 2 cm
Arm Type
Experimental
Arm Description
Sleeve gastrectomy with a 33Fr bougie size and 2 cm distance from the pylorus.
Arm Title
Bougie Size 33Fr Distance pylorus 5 cm
Arm Type
Experimental
Arm Description
Sleeve gastrectomy with a 33Fr bougie size and 5 cm distance from the pylorus
Arm Title
Bougie Size 42Fr Distance pylorus 2 cm
Arm Type
Experimental
Arm Description
Sleeve gastrectomy with a 42Fr bougie size and 2 cm distance from the pylorus
Arm Title
Bougie Size 42Fr Distance pylorus 5 cm
Arm Type
Experimental
Arm Description
Sleeve gastrectomy with a 42Fr bougie size and 2 cm distance from the pylorus
Intervention Type
Procedure
Intervention Name(s)
Bougie Size 33 Fr
Intervention Description
Comparison of the bougie size and distance from the pylorus for the sleeve gastrectomy
Intervention Type
Procedure
Intervention Name(s)
Bougie Size 42 Fr
Intervention Description
Comparison of the bougie size and distance from the pylorus for the sleeve gastrectomy
Intervention Type
Procedure
Intervention Name(s)
Distance pylorus 2 cm
Intervention Description
Comparison of the bougie size and distance from the pylorus for the sleeve gastrectomy
Intervention Type
Procedure
Intervention Name(s)
Distance pylorus 5 cm
Intervention Description
Comparison of the bougie size and distance from the pylorus for the sleeve gastrectomy
Primary Outcome Measure Information:
Title
Body mass index
Time Frame
1 year
Title
Gastric volume
Time Frame
1 month and 1 year
Secondary Outcome Measure Information:
Title
Gastric emptying time
Time Frame
1 year
Title
Lower esophageal sphincter pressure
Time Frame
1 year
Title
Number of gastroesophageal reflux episodes
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Hormone levels
Description
Insulin, Glucagon, glucagon-like peptide (GLP-1), gastric inhibitory peptide (GIP), Ghrelin, Leptin, Adiponectin, Peptide YY
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age more than 18 years and less than 65 years BMI more than 40 kg/m2 or more than 35 kg/m2 with comorbidities likely to improve after weight loss. Morbid obesity established at least five years. Continued failures to adequately supervised conservative treatments Absence of endocrine disorders that are due to morbid obesity. Psychological stability: No alcohol or drug abuse. Absence of major psychiatric disorders (schizophrenia, psychosis), mental retardation, eating disorders (bulimia nervosa). Ability to understand the mechanisms to lose weight with surgery and understand that not always achieved good results. Understand that the goal of surgery is to achieve the ideal weight. Commitment for Adherence to surveillance guidelines after surgery Informed consent after receiving all the necessary information (oral and written). Women of childbearing age should avoid pregnancy for at least the first year after surgery Exclusion Criteria: No acceptance Age less than 18 years or more than 65 years Previous bariatric surgery Previous gastric surgery Inflammatory bowel disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Carmen Balagué Ponz, MD
Phone
+34 935565671
Email
cbalague@santpau.cat
First Name & Middle Initial & Last Name or Official Title & Degree
Eduardo Maria Targarona Soler, MD PhD
Phone
+34 935565671
Email
etargarona@santpau.cat
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Carmen Balagué Ponz, MD
Organizational Affiliation
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
ZIP/Postal Code
08025
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Carmen Balagué Ponz, MD
Phone
+34 93 556 56 71
Email
cbalague@santpau.cat
First Name & Middle Initial & Last Name & Degree
Eduardo Maria Targarona Soler, MD PhD
Phone
+34 93 556 56 71
Email
etargarona@santpau.cat
First Name & Middle Initial & Last Name & Degree
Eduardo Maria Targarona Soler, MD PhD

12. IPD Sharing Statement

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Impact of Size of Gastric Sleeve on the Weight Loss. Correlation With Gastric Function and Endocrine-metabolic Changes.

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