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Preoperative Condition in Giant Obese Patients

Primary Purpose

Morbid Obesity, Bariatric Surgery Candidate

Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Liraglutide
Aminosteril hepa 8%
Caloric diet with 1000 kcal
Sponsored by
Sana Klinikum Offenbach
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Morbid Obesity focused on measuring Morbid Obesity, Giant Obese, Preoperative Procedure, Liraglutide, Leucine

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • multimorbid, super-super obese patients

Exclusion Criteria:

  • renal insufficiency III

Sites / Locations

  • Sana Klinikum Offenbach

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Super-super Obese Patients

Arm Description

Multimorbid, super-super obese patients that need preoperative conditioning therapy (intervention 1: Liraglutide, intervention 2: aminosteril hepa 8%, intervention 3: Caloric diet with 1000 kcal) for weight loss surgery to achieve technical operability.

Outcomes

Primary Outcome Measures

Operability
Operability means that weight loss surgery could be performed after preoperative condition (due to less visceral fat, less liver volume)

Secondary Outcome Measures

Chronic inflammation
Changing in CRP in g/l during intervention
Chronic inflammation II
Changing in white blood cell count /nl during intervention
Liver volume
Changing of liver volume during intervention measured by ultrasound
Liver function
Changing of GOT in U/l, GPT in U/l, GGT in U/l and AP in U/l
Pulmonary function
Changing in FEV1 in lung function testing during intervention
Hg A1c in %
Total Protein in g/l
Preoperative excess weight loss in %
Albumin in g/l

Full Information

First Posted
November 17, 2015
Last Updated
March 21, 2021
Sponsor
Sana Klinikum Offenbach
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1. Study Identification

Unique Protocol Identification Number
NCT02616003
Brief Title
Preoperative Condition in Giant Obese Patients
Official Title
A Novel Preoperative Conditioning Therapy in Giant Obese Patients With the Combination of Liraglutide and a Leucine-Based Amino-Acid Infusion and Caloric Restriction
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
April 2014 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
April 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sana Klinikum Offenbach

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The frequency of super-super obese who need immediate weight loss surgery is risen continuously. For those patients a prior-to-surgery conditioning therapy is mandatory to gain technical and physical operability. The exclusively well-established preliminary therapy so far was the intragastric balloon, which takes 7 months of treatment time. Due to life-threatening conditions of giant obese patients, who have been admitted to hospital, the investigators were forced to develop a more prompt acting conditioning therapy to bring those individuals in a short run to an improved and "fit-for-surgery" state. In such an impasse the investigators combine Liraglutide with its well-known weight-loss effect with a leucine-based amino acid infusion that is generally used for patients with liver insufficiency, in expectance of an additional weight loss and liver reduction effect.
Detailed Description
The investigators will use a commercial available amino acid infusion (Aminosteril hepa 8%, Fresenius Karbi), which is used in clinical application for liver conditioning. It is mainly based on the branched-chained amino acid leucine (13.09 g per 1000 ml). The investigators will combine this with a daily subcutaneous injection of Liraglutide. Liraglutide is a GLP-1 analogue, which achieved meanwhile the FDA approval for weight loss treatment. Initial Liraglutide dosage is 1.2 mg for three days, boosted to 1.8 mg consecutively. Participants receive energy reduced nutrition with 1000 kcal/d.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morbid Obesity, Bariatric Surgery Candidate
Keywords
Morbid Obesity, Giant Obese, Preoperative Procedure, Liraglutide, Leucine

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Super-super Obese Patients
Arm Type
Other
Arm Description
Multimorbid, super-super obese patients that need preoperative conditioning therapy (intervention 1: Liraglutide, intervention 2: aminosteril hepa 8%, intervention 3: Caloric diet with 1000 kcal) for weight loss surgery to achieve technical operability.
Intervention Type
Drug
Intervention Name(s)
Liraglutide
Other Intervention Name(s)
Victoza
Intervention Description
Initially 1.2 mg Liraglutide as subcutaneous daily injection, boosted to 1.8 mg Liraglutide after 3 days subsequently. 1000 ml infusion of aminosteril hepa 8% from day 1 onwards. Caloric diet with 800 kcal from day 1 onwards till technical operability is achieved (about 21 days)
Intervention Type
Other
Intervention Name(s)
Aminosteril hepa 8%
Intervention Description
Initially 1.2 mg Liraglutide as subcutaneous daily injection, boosted to 1.8 mg Liraglutide after 3 days subsequently. 1000 ml infusion of aminosteril hepa 8% from day 1 onwards. Caloric diet with 800 kcal from day 1 onwards till technical operability is achieved (about 21 days)
Intervention Type
Dietary Supplement
Intervention Name(s)
Caloric diet with 1000 kcal
Intervention Description
Initially 1.2 mg Liraglutide as subcutaneous daily injection, boosted to 1.8 mg Liraglutide after 3 days subsequently. 1000 ml infusion of aminosteril hepa 8% from day 1 onwards. Caloric diet with 1000 kcal from day 1 onwards till technical operability is achieved (about 21 days)
Primary Outcome Measure Information:
Title
Operability
Description
Operability means that weight loss surgery could be performed after preoperative condition (due to less visceral fat, less liver volume)
Time Frame
21 days
Secondary Outcome Measure Information:
Title
Chronic inflammation
Description
Changing in CRP in g/l during intervention
Time Frame
21 days
Title
Chronic inflammation II
Description
Changing in white blood cell count /nl during intervention
Time Frame
21 days
Title
Liver volume
Description
Changing of liver volume during intervention measured by ultrasound
Time Frame
21 days
Title
Liver function
Description
Changing of GOT in U/l, GPT in U/l, GGT in U/l and AP in U/l
Time Frame
21 days
Title
Pulmonary function
Description
Changing in FEV1 in lung function testing during intervention
Time Frame
21 days
Title
Hg A1c in %
Time Frame
21 days
Title
Total Protein in g/l
Time Frame
21 days
Title
Preoperative excess weight loss in %
Time Frame
21 days
Title
Albumin in g/l
Time Frame
21 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: multimorbid, super-super obese patients Exclusion Criteria: renal insufficiency III
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rudolf Weiner, MD, Prof.
Organizational Affiliation
Sana Klinikum Offenbach
Official's Role
Study Chair
Facility Information:
Facility Name
Sana Klinikum Offenbach
City
Offenbach
State/Province
Hessen
ZIP/Postal Code
63069
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
25202976
Citation
Baggio LL, Drucker DJ. Glucagon-like peptide-1 receptors in the brain: controlling food intake and body weight. J Clin Invest. 2014 Oct;124(10):4223-6. doi: 10.1172/JCI78371. Epub 2014 Sep 9.
Results Reference
result
PubMed Identifier
24681814
Citation
Alhadeff AL, Baird JP, Swick JC, Hayes MR, Grill HJ. Glucagon-like Peptide-1 receptor signaling in the lateral parabrachial nucleus contributes to the control of food intake and motivation to feed. Neuropsychopharmacology. 2014 Aug;39(9):2233-43. doi: 10.1038/npp.2014.74. Epub 2014 Mar 26.
Results Reference
result
PubMed Identifier
26132939
Citation
Pi-Sunyer X, Astrup A, Fujioka K, Greenway F, Halpern A, Krempf M, Lau DC, le Roux CW, Violante Ortiz R, Jensen CB, Wilding JP; SCALE Obesity and Prediabetes NN8022-1839 Study Group. A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management. N Engl J Med. 2015 Jul 2;373(1):11-22. doi: 10.1056/NEJMoa1411892.
Results Reference
result
PubMed Identifier
26007339
Citation
Pedroso JA, Zampieri TT, Donato J Jr. Reviewing the Effects of L-Leucine Supplementation in the Regulation of Food Intake, Energy Balance, and Glucose Homeostasis. Nutrients. 2015 May 22;7(5):3914-37. doi: 10.3390/nu7053914.
Results Reference
result
PubMed Identifier
17360978
Citation
Zhang Y, Guo K, LeBlanc RE, Loh D, Schwartz GJ, Yu YH. Increasing dietary leucine intake reduces diet-induced obesity and improves glucose and cholesterol metabolism in mice via multimechanisms. Diabetes. 2007 Jun;56(6):1647-54. doi: 10.2337/db07-0123. Epub 2007 Mar 14.
Results Reference
result
PubMed Identifier
22535285
Citation
McAllan L, Cotter PD, Roche HM, Korpela R, Nilaweera KN. Impact of leucine on energy balance. J Physiol Biochem. 2013 Mar;69(1):155-63. doi: 10.1007/s13105-012-0170-2. Epub 2012 Apr 26.
Results Reference
result
PubMed Identifier
35871930
Citation
Stier C, Koschker AC, Kim M, Stier R, Chiappetta S, Stein J. Fast-track rescue weight reduction therapy to achieve rapid technical operability for emergency bariatric surgery in patients with life-threatening inoperable severe obesity - A proof of concept study. Clin Nutr ESPEN. 2022 Aug;50:238-246. doi: 10.1016/j.clnesp.2022.05.009. Epub 2022 May 26.
Results Reference
derived

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Preoperative Condition in Giant Obese Patients

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