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Gastric Bypass, Gastric Band or Sleeve Gastrectomy to Treat Obesity (ByBandSleeve)

Primary Purpose

Obesity, Surgery, Quality of Life

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Gastric Band
Gastric Bypass
Sleeve Gastrectomy
Sponsored by
University of Bristol
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

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

Inclusion Criteria:

  1. Male or female patients
  2. Over 18 years of age
  3. Referred for bariatric surgery according to the National Institute for Health and Care Excellence (NICE) guidelines - BMI of 40kg/m2 or more, OR BMI of 35 kg/m2 to 40 kg/m2 and other significant disease (e.g. type 2 diabetes or high blood pressure) OR BMI of 30 kg/m2 or more and recent onset diabetes OR Asian family origin with lower BMI and recent onset diabetes, that could improve with weight loss
  4. Has been or is willing to receive intensive management in a specialist tier 3 obesity service
  5. Fit for anaesthesia and surgery
  6. Committed to follow-up and able to complete quality of life questionnaires
  7. Able to provide written informed consent.

Exclusion Criteria:

  1. Previous gastric surgery or surgery for severe and complex obesity
  2. Previous abdominal surgery or gastro-intestinal (GI) condition that precludes one or more of Band, Bypass or Sleeve
  3. Large abdominal ventral hernia
  4. Pregnancy (women who have given birth and women planning pregnancy will NOT be excluded)
  5. Crohn's disease
  6. Liver cirrhosis and portal hypertension
  7. Systemic lupus erythematosis
  8. Known silicone allergy
  9. Hiatus hernia >5cm
  10. Other clinical/psychological reason, to be specified
  11. Active participation in another interventional research study which might interfere with By-Band-Sleeve

Sites / Locations

  • Heart of England NHS Foundation Trust
  • Royal Bournemouth and Christchurch Hospitals
  • North Bristol NHS Trust
  • Royal Derby Hospital
  • St James University Hospital, Leeds
  • Homerton University Hospital
  • Imperial College Healthcare NHS Trust
  • Queen Alexandra Hospital
  • University Hospital Southampton
  • Sunderland Royal Hospital
  • Musgrove Park Hospital
  • Royal Cornwall Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Gastric Band

Gastric Bypass

Sleeve Gastrectomy

Arm Description

The procedure will involve an operation in which a gastric Band and port will be fitted using a laparoscopic technique.

The procedure will involve a laparoscopic operation in which a small pouch is made in the top of the stomach and a loop of bowel connected to this pouch to bypass the rest of the stomach.

The procedure involves an operation which reduces the size of the stomach by about 75%, creating a narrow tube. It is done by stapling down the stomach and removing the remainder of the stomach using a laparoscopic technique.

Outcomes

Primary Outcome Measures

The proportion achieving loss of greater than 50% of excess weight at three years.
The proportion achieving loss of greater than 50% of excess weight at three years (calculated as 100×[BMI at 3 years - BMI at randomisation1] / [BMI at randomisation - 25])
Health-related Quality of Life (HRQoL)
HRQoL at three 3 years, will be assessed using the EQ-5D-5L

Secondary Outcome Measures

Change in BMI over time adjusted for BMI at randomisation
Change in BMI over time adjusted for BMI at randomisation
Percentage weight loss at 3 years
Percentage weight loss at 3 years
Waist circumference at 3 years
Waist circumference at 3 years
Time taken from randomisation to reach first loss of at least 50% of excess BMI
Time taken from randomisation to reach first loss of at least 50% of excess BMI
Time taken from first losing 50% excess BMI to first relapse
Time taken from first losing 50% excess BMI to first relapse (defined as weight re-gain such that the target of at least 50% of excess weight loss is no longer met)
Generic and symptom specific Health-related Quality of Life (HRQOL)
Impact of Weight on Quality of Life (IWQOL-Lite)
Generic and symptom specific Health-related Quality of Life (HRQOL)
The Gastrointestinal Quality of Life Index
Generic and symptom specific Health-related Quality of Life (HRQOL)
Eating Habits Questionnaire
Generic and symptom specific Health-related Quality of Life (HRQOL)
SF-12v2 Health Survey
Generic and symptom specific Health-related Quality of Life (HRQOL)
Hospital Anxiety and Depression Scale (HADS).
Resource use to three years
Use of health service resources over the three-year study period.
Standard healthcare blood tests
Standard NHS nutritional blood tests will be performed at each assessment.
Dietary recall
Measures of 24 hour recall eating using a standardised and validated interview process
Binge eating behaviour
Binge eating behaviour using a validated questionnaire
Adverse health events
Adverse health events including the need for re-operation and cross over between interventions
Resolution of co-morbidities
Resolution of co-morbidities at 3 years, including sleep apnoea, non alcoholic fatty liver disease, type-2 diabetes, hypertension and hyperlipidaemia.
Time to resolution of co-morbidities
Time to resolution of sleep apnoea, type-2 diabetes, hypertension and hyperlipidaemia

Full Information

First Posted
April 8, 2016
Last Updated
May 11, 2023
Sponsor
University of Bristol
Collaborators
University of Oxford, University of Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT02841527
Brief Title
Gastric Bypass, Gastric Band or Sleeve Gastrectomy to Treat Obesity
Acronym
ByBandSleeve
Official Title
Gastric Bypass, Adjustable Gastric Banding or Sleeve Gastrectomy Surgery to Treat Severe and Complex Obesity: a Multi-centre Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
January 1, 2012 (Actual)
Primary Completion Date
September 30, 2022 (Actual)
Study Completion Date
March 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bristol
Collaborators
University of Oxford, University of Birmingham

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Obesity is an increasing health problem in the United Kingdom (UK) and is predicted to worsen. In the UK and worldwide the three most commonly performed operations are laparoscopic adjustable gastric banding ('BAND surgery'), laparoscopic gastric bypass ('BYPASS') and laparoscopic sleeve gastrectomy ('SLEEVE'). All lead to weight loss, but they are associated with different problems. This study (BYBANDSLEEVE) is a randomised trial with a target recruitment of 1341 patients in twelve hospitals and its aim is to compare the effectiveness, cost effectiveness and acceptability of BAND, BYPASS and SLEEVE surgery.
Detailed Description
Obesity is an increasing health problem in the UK and one which is predicted to worsen. It is associated with many health problems that can shorten a person's life span and impair quality of life. Current national guidelines recommend that surgery is considered for the very overweight (morbidly obese) or for those remaining obese after trying other options. In the UK and worldwide the three most commonly performed operations are laparoscopic adjustable gastric banding ('BAND surgery'), laparoscopic gastric bypass ('BYPASS') and laparoscopic sleeve gastrectomy ('SLEEVE'). All lead to weight loss, but they are associated with different problems. In the short term there are varying complications and inconvenience relating to the operation. In the longer term there are different outcomes relating to weight regain, symptoms and side effects of surgery. This study (BYBANDSLEEVE) is a randomised trial with a recruitment target of 1341 patients in twelve hospitals and its aim is to compare the effectiveness, cost effectiveness and acceptability of BAND, BYPASS and SLEEVE surgery. The process of randomisation will mean that participants have a chance of receiving one of the three procedures, so a fair comparison between them can be made. The first phase (in two hospitals) will test the feasibility of recruitment and optimise information for patients to maximise trial recruitment. It will establish a core set of clinical outcomes to use to evaluate the surgery for morbid obesity. The second stage (in 12 hospitals) will recruit the full sample and follow up all participants for at least three years. The investigators will compare the effects of BAND, BYPASS AND SLEEVE surgery three years after randomisation on weight loss, a wide range of symptoms and aspects of quality of life. The investigators will also examine patients' detailed experiences during follow up, nutritional outcomes, short and long term surgical complications and National Health Service (NHS) value for money.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Surgery, Quality of Life, Weight Loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1351 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Gastric Band
Arm Type
Active Comparator
Arm Description
The procedure will involve an operation in which a gastric Band and port will be fitted using a laparoscopic technique.
Arm Title
Gastric Bypass
Arm Type
Active Comparator
Arm Description
The procedure will involve a laparoscopic operation in which a small pouch is made in the top of the stomach and a loop of bowel connected to this pouch to bypass the rest of the stomach.
Arm Title
Sleeve Gastrectomy
Arm Type
Active Comparator
Arm Description
The procedure involves an operation which reduces the size of the stomach by about 75%, creating a narrow tube. It is done by stapling down the stomach and removing the remainder of the stomach using a laparoscopic technique.
Intervention Type
Procedure
Intervention Name(s)
Gastric Band
Intervention Description
Surgical intervention in which a band is inserted around the top of the stomach to reduce its size.
Intervention Type
Procedure
Intervention Name(s)
Gastric Bypass
Intervention Description
Surgical intervention where a small pouch is made in the top of the stomach and a loop of bowel connected to this pouch to bypass the rest of the stomach.
Intervention Type
Procedure
Intervention Name(s)
Sleeve Gastrectomy
Intervention Description
Surgical intervention which reduces the size of the stomach by about 75%, creating a narrow tube. It is done by stapling down the stomach and removing the remainder of the stomach.
Primary Outcome Measure Information:
Title
The proportion achieving loss of greater than 50% of excess weight at three years.
Description
The proportion achieving loss of greater than 50% of excess weight at three years (calculated as 100×[BMI at 3 years - BMI at randomisation1] / [BMI at randomisation - 25])
Time Frame
Three years
Title
Health-related Quality of Life (HRQoL)
Description
HRQoL at three 3 years, will be assessed using the EQ-5D-5L
Time Frame
Three years
Secondary Outcome Measure Information:
Title
Change in BMI over time adjusted for BMI at randomisation
Description
Change in BMI over time adjusted for BMI at randomisation
Time Frame
Three years
Title
Percentage weight loss at 3 years
Description
Percentage weight loss at 3 years
Time Frame
Three years
Title
Waist circumference at 3 years
Description
Waist circumference at 3 years
Time Frame
Three years
Title
Time taken from randomisation to reach first loss of at least 50% of excess BMI
Description
Time taken from randomisation to reach first loss of at least 50% of excess BMI
Time Frame
Three years
Title
Time taken from first losing 50% excess BMI to first relapse
Description
Time taken from first losing 50% excess BMI to first relapse (defined as weight re-gain such that the target of at least 50% of excess weight loss is no longer met)
Time Frame
Three years
Title
Generic and symptom specific Health-related Quality of Life (HRQOL)
Description
Impact of Weight on Quality of Life (IWQOL-Lite)
Time Frame
Three years
Title
Generic and symptom specific Health-related Quality of Life (HRQOL)
Description
The Gastrointestinal Quality of Life Index
Time Frame
Three years
Title
Generic and symptom specific Health-related Quality of Life (HRQOL)
Description
Eating Habits Questionnaire
Time Frame
Three years
Title
Generic and symptom specific Health-related Quality of Life (HRQOL)
Description
SF-12v2 Health Survey
Time Frame
Three years
Title
Generic and symptom specific Health-related Quality of Life (HRQOL)
Description
Hospital Anxiety and Depression Scale (HADS).
Time Frame
Three years
Title
Resource use to three years
Description
Use of health service resources over the three-year study period.
Time Frame
Three years
Title
Standard healthcare blood tests
Description
Standard NHS nutritional blood tests will be performed at each assessment.
Time Frame
Three years
Title
Dietary recall
Description
Measures of 24 hour recall eating using a standardised and validated interview process
Time Frame
Three years
Title
Binge eating behaviour
Description
Binge eating behaviour using a validated questionnaire
Time Frame
Three years
Title
Adverse health events
Description
Adverse health events including the need for re-operation and cross over between interventions
Time Frame
Three years
Title
Resolution of co-morbidities
Description
Resolution of co-morbidities at 3 years, including sleep apnoea, non alcoholic fatty liver disease, type-2 diabetes, hypertension and hyperlipidaemia.
Time Frame
Three years
Title
Time to resolution of co-morbidities
Description
Time to resolution of sleep apnoea, type-2 diabetes, hypertension and hyperlipidaemia
Time Frame
Three years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female patients Over 18 years of age Referred for bariatric surgery according to the National Institute for Health and Care Excellence (NICE) guidelines - BMI of 40kg/m2 or more, OR BMI of 35 kg/m2 to 40 kg/m2 and other significant disease (e.g. type 2 diabetes or high blood pressure) OR BMI of 30 kg/m2 or more and recent onset diabetes OR Asian family origin with lower BMI and recent onset diabetes, that could improve with weight loss Has been or is willing to receive intensive management in a specialist tier 3 obesity service Fit for anaesthesia and surgery Committed to follow-up and able to complete quality of life questionnaires Able to provide written informed consent. Exclusion Criteria: Previous gastric surgery or surgery for severe and complex obesity Previous abdominal surgery or gastro-intestinal (GI) condition that precludes one or more of Band, Bypass or Sleeve Large abdominal ventral hernia Pregnancy (women who have given birth and women planning pregnancy will NOT be excluded) Crohn's disease Liver cirrhosis and portal hypertension Systemic lupus erythematosis Known silicone allergy Hiatus hernia >5cm Other clinical/psychological reason, to be specified Active participation in another interventional research study which might interfere with By-Band-Sleeve
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jane Blazeby, BSc,MBChB,MD
Organizational Affiliation
University of Bristol
Official's Role
Study Director
Facility Information:
Facility Name
Heart of England NHS Foundation Trust
City
Birmingham
Country
United Kingdom
Facility Name
Royal Bournemouth and Christchurch Hospitals
City
Bournemouth
Country
United Kingdom
Facility Name
North Bristol NHS Trust
City
Bristol
Country
United Kingdom
Facility Name
Royal Derby Hospital
City
Derby
Country
United Kingdom
Facility Name
St James University Hospital, Leeds
City
Leeds
Country
United Kingdom
Facility Name
Homerton University Hospital
City
London
Country
United Kingdom
Facility Name
Imperial College Healthcare NHS Trust
City
London
Country
United Kingdom
Facility Name
Queen Alexandra Hospital
City
Portsmouth
Country
United Kingdom
Facility Name
University Hospital Southampton
City
Southampton
Country
United Kingdom
Facility Name
Sunderland Royal Hospital
City
Sunderland
Country
United Kingdom
Facility Name
Musgrove Park Hospital
City
Taunton
Country
United Kingdom
Facility Name
Royal Cornwall Hospital
City
Truro
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
All data will be anonymised and analysed in groups. Individual patient data (IPD) will be made available to the research team following analysis.
Citations:
PubMed Identifier
24633209
Citation
Blazeby JM, Byrne J, Welbourn R. What is the most effective operation for adults with severe and complex obesity? BMJ. 2014 Mar 14;348:g1763. doi: 10.1136/bmj.g1763. No abstract available.
Results Reference
background
PubMed Identifier
24393291
Citation
Donovan JL, Paramasivan S, de Salis I, Toerien M. Clear obstacles and hidden challenges: understanding recruiter perspectives in six pragmatic randomised controlled trials. Trials. 2014 Jan 6;15:5. doi: 10.1186/1745-6215-15-5.
Results Reference
background
PubMed Identifier
24517309
Citation
Rogers CA, Welbourn R, Byrne J, Donovan JL, Reeves BC, Wordsworth S, Andrews R, Thompson JL, Roderick P, Mahon D, Noble H, Kelly J, Mazza G, Pike K, Paramasivan S, Blencowe N, Perkins M, Porter T, Blazeby JM. The By-Band study: gastric bypass or adjustable gastric band surgery to treat morbid obesity: study protocol for a multi-centre randomised controlled trial with an internal pilot phase. Trials. 2014 Feb 11;15:53. doi: 10.1186/1745-6215-15-53.
Results Reference
background
PubMed Identifier
25442513
Citation
Hopkins JC, Howes N, Chalmers K, Savovic J, Whale K, Coulman KD, Welbourn R, Whistance RN, Andrews RC, Byrne JP, Mahon D, Blazeby JM; By-Band Trial Management Group. Outcome reporting in bariatric surgery: an in-depth analysis to inform the development of a core outcome set, the BARIACT Study. Obes Rev. 2015 Jan;16(1):88-106. doi: 10.1111/obr.12240. Epub 2014 Nov 30.
Results Reference
background
PubMed Identifier
27898680
Citation
Coulman KD, Hopkins J, Brookes ST, Chalmers K, Main B, Owen-Smith A, Andrews RC, Byrne J, Donovan JL, Mazza G, Reeves BC, Rogers CA, Thompson JL, Welbourn R, Wordsworth S, Blazeby JM; BARIACT working group. A Core Outcome Set for the Benefits and Adverse Events of Bariatric and Metabolic Surgery: The BARIACT Project. PLoS Med. 2016 Nov 29;13(11):e1002187. doi: 10.1371/journal.pmed.1002187. eCollection 2016 Nov.
Results Reference
background
PubMed Identifier
27138600
Citation
Coulman KD, Howes N, Hopkins J, Whale K, Chalmers K, Brookes S, Nicholson A, Savovic J, Ferguson Y, Owen-Smith A, Blazeby J; By-Band-Sleeve Trial Management Group; Blazeby J, Welbourn R, Byrne J, Donovan J, Reeves BC, Wordsworth S, Andrews R, Thompson JL, Mazza G, Rogers CA. A Comparison of Health Professionals' and Patients' Views of the Importance of Outcomes of Bariatric Surgery. Obes Surg. 2016 Nov;26(11):2738-2746. doi: 10.1007/s11695-016-2186-0.
Results Reference
background
PubMed Identifier
27034443
Citation
Hopkins JC, Blazeby JM, Rogers CA, Welbourn R. The use of adjustable gastric bands for management of severe and complex obesity. Br Med Bull. 2016 Jun;118(1):64-72. doi: 10.1093/bmb/ldw012. Epub 2016 Mar 31.
Results Reference
background
PubMed Identifier
27755555
Citation
Rooshenas L, Elliott D, Wade J, Jepson M, Paramasivan S, Strong S, Wilson C, Beard D, Blazeby JM, Birtle A, Halliday A, Rogers CA, Stein R, Donovan JL; ACST-2 study group; By-Band-Sleeve study group; Chemorad study group; CSAW study group; Optima prelim study group; POUT study group. Conveying Equipoise during Recruitment for Clinical Trials: Qualitative Synthesis of Clinicians' Practices across Six Randomised Controlled Trials. PLoS Med. 2016 Oct 18;13(10):e1002147. doi: 10.1371/journal.pmed.1002147. eCollection 2016 Oct.
Results Reference
background
PubMed Identifier
27169605
Citation
Welbourn R, le Roux CW, Owen-Smith A, Wordsworth S, Blazeby JM. Why the NHS should do more bariatric surgery; how much should we do? BMJ. 2016 May 11;353:i1472. doi: 10.1136/bmj.i1472. No abstract available.
Results Reference
background
PubMed Identifier
28550438
Citation
Doble B, Wordsworth S, Rogers CA, Welbourn R, Byrne J, Blazeby JM; By-Band-Sleeve Trial Management Group. What Are the Real Procedural Costs of Bariatric Surgery? A Systematic Literature Review of Published Cost Analyses. Obes Surg. 2017 Aug;27(8):2179-2192. doi: 10.1007/s11695-017-2749-8. Erratum In: Obes Surg. 2017 Aug;27(8):2193.
Results Reference
background
PubMed Identifier
29252996
Citation
Fermont JM, Blazeby JM, Rogers CA, Wordsworth S; By-Band-Sleeve Study Management Group. The EQ-5D-5L is a valid approach to measure health related quality of life in patients undergoing bariatric surgery. PLoS One. 2017 Dec 18;12(12):e0189190. doi: 10.1371/journal.pone.0189190. eCollection 2017.
Results Reference
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PubMed Identifier
28669987
Citation
Paramasivan S, Rogers CA, Welbourn R, Byrne JP, Salter N, Mahon D, Noble H, Kelly J, Mazza G, Whybrow P, Andrews RC, Wilson C, Blazeby JM, Donovan JL. Enabling recruitment success in bariatric surgical trials: pilot phase of the By-Band-Sleeve study. Int J Obes (Lond). 2017 Nov;41(11):1654-1661. doi: 10.1038/ijo.2017.153. Epub 2017 Jul 3.
Results Reference
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PubMed Identifier
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Citation
Rogers CA, Reeves BC, Byrne J, Donovan JL, Mazza G, Paramasivan S, Andrews RC, Wordsworth S, Thompson J, Blazeby JM, Welbourn R; By-Band-Sleeve study investigators. Adaptation of the By-Band randomized clinical trial to By-Band-Sleeve to include a new intervention and maintain relevance of the study to practice. Br J Surg. 2017 Aug;104(9):1207-1214. doi: 10.1002/bjs.10562.
Results Reference
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PubMed Identifier
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Citation
Doble B, Welbourn R, Carter N, Byrne J, Rogers CA, Blazeby JM, Wordsworth S; By-Band-Sleeve Trial Management Group. Multi-Centre Micro-Costing of Roux-En-Y Gastric Bypass, Sleeve Gastrectomy and Adjustable Gastric Banding Procedures for the Treatment of Severe, Complex Obesity. Obes Surg. 2019 Feb;29(2):474-484. doi: 10.1007/s11695-018-3553-9.
Results Reference
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PubMed Identifier
30339938
Citation
Rooshenas L, Scott LJ, Blazeby JM, Rogers CA, Tilling KM, Husbands S, Conefrey C, Mills N, Stein RC, Metcalfe C, Carr AJ, Beard DJ, Davis T, Paramasivan S, Jepson M, Avery K, Elliott D, Wilson C, Donovan JL; By-Band-Sleeve study group; CSAW study group; HAND-1 study group; Optima prelim study group; Romio feasibility study group. The QuinteT Recruitment Intervention supported five randomized trials to recruit to target: a mixed-methods evaluation. J Clin Epidemiol. 2019 Feb;106:108-120. doi: 10.1016/j.jclinepi.2018.10.004. Epub 2018 Oct 16.
Results Reference
background
Links:
URL
http://www.by-band-sleeve.bristol.ac.uk/
Description
By-Band-Sleeve study website

Learn more about this trial

Gastric Bypass, Gastric Band or Sleeve Gastrectomy to Treat Obesity

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