Obesity Clinical Trial
— PBSOfficial title:
National Patient-Centered Clinical Research Network (PCORnet) Bariatric Study
NCT number | NCT02741674 |
Other study ID # | OBS-1505-30683 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | February 2016 |
Est. completion date | April 30, 2018 |
Verified date | December 2023 |
Source | Kaiser Permanente |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The main goal of this research project is to conduct a comparative effectiveness research study involving existing data in the PCORnet Common Data Model to provide accurate estimates of the 1-, 3-, and 5-year benefits and risks of the three most common bariatric procedures - Roux-en-y gastric bypass, adjustable gastric banding, and sleeve gastrectomy - with a focus on outcomes that are important to adults and adolescents with severe obesity: 1) changes in weight, 2) rates of remission and relapse of diabetes, and 3) major adverse events.
Status | Completed |
Enrollment | 65093 |
Est. completion date | April 30, 2018 |
Est. primary completion date | April 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 12 Years to 79 Years |
Eligibility | ALL STUDY AIMS - Inclusion Criteria: - Adults and children ages 12 =79 years at time of surgery - Had a primary (not revision) bariatric procedure from years 2005-2015 of one of three types: 1. Roux-en-y gastric bypass (RYGB) 2. Adjustable gastric banding (AGB) 3. Sleeve gastrectomy (SG) - Have a Body Mass Index (BMI) measurement in the year prior to surgery that is =35 kg/m2 - Exclusion Criteria: - First bariatric procedure during the study period is a revision procedure, a vertical banded gastroplasty procedure or Biliopancreatic Diversion Procedure - Have multiple bariatric procedures coded on the same day - Have a diagnosis related to GI cancer occurring on day of surgery or during index hospitalization (Diagnosis determined using International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) - Emergency department visit on the same day as hospitalization for bariatric procedure ADDITIONAL INCLUSION CRITERIA FOR AIM 2 (Diabetes) • Eligible patients must have uncontrolled or medication-controlled diabetes at the time of surgery. - Hemoglobin A1c (HbA1c) =6.5 % at the most recent measurement prior to surgery, or - Current prescription for diabetes medication at the time of surgery with the most recent HbA1c <6.5% Patients taking only metformin will be excluded unless they also have an ICD-9-CM code for Diabetes (250.x) or have HbA1c >=6.5% in the year prior to surgery. This includes patients with polycystic ovarian syndrome (PCOS). ADDITIONAL INCLUSION CRITERIA FOR AIM 3 (Adverse Events) - Eligible patients must be linked to relevant data sources: - State or national death index (mortality outcomes); - Payer data/insurance claims (for Adverse Events outcomes) - Patients must be aged 20 through 79 years of age at time of surgery. ADDITIONAL EXCLUSION CRITIERA FOR AIM 3 (Adverse Events) - Exclude any patient with >=365 inpatient hospitalization days in the year prior to surgery. - Exclude any patient without male or female sex indicated in the study data AIM 4 (Surgery Outcomes and Baseline Depression) and AIM 5 (Surgery Outcomes and Race/Ethnicity): Inclusion criteria for Aims 1, 2, and 3 will be used for the outcomes from these aims. ADDITIONAL INCLUSION CRITERIA FOR AIM 5 (Surgery Outcomes and Race/Ethnicity) • Race and ethnicity available in study data |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Kaiser Permanente | Chicago Area Patient-Centered Outcomes Research Network (CAPriCORN), COPD Patient-Powered Research Network, Greater Plains Collaborative Clinical Data Research Network, Harvard Pilgrim Health Care, Mid-South Clinical Data Research Network, National Patient-Centered Clinical Research Network, New York City Clinical Data Research Network, Obesity Action Coalition, OneFlorida Clinical Research Consortium, PaTH: Towards a Learning Health System Clinical Data Research Network, Patient-Centered Outcomes Research Institute, Patient-Centered SCAlable National Network for Effectiveness Research (pSCANNER), PEDSnet: A Pediatric Learning Health System CDRN, Research Action for Health Network (REACHnet), Scalable Collaborative Infrastructure for a Learning Healthcare System (SCILHS) |
Arterburn D, Wellman R, Emiliano A, Smith SR, Odegaard AO, Murali S, Williams N, Coleman KJ, Courcoulas A, Coley RY, Anau J, Pardee R, Toh S, Janning C, Cook A, Sturtevant J, Horgan C, McTigue KM; PCORnet Bariatric Study Collaborative. Comparative Effecti — View Citation
Coleman KJ, Wellman R, Fitzpatrick SL, Conroy MB, Hlavin C, Lewis KH, Coley RY, McTigue KM, Tobin JN, McBride CL, Desai JR, Clark JM, Toh S, Sturtevant JL, Horgan CE, Duke MC, Williams N, Anau J, Horberg MA, Michalsky MP, Cook AJ, Arterburn DE, Apovian CM — View Citation
Coughlin JW, Nauman E, Wellman R, Coley RY, McTigue KM, Coleman KJ, Jones DB, Lewis KH, Tobin JN, Wee CC, Fitzpatrick SL, Desai JR, Murali S, Morrow EH, Rogers AM, Wood GC, Schlundt DG, Apovian CM, Duke MC, McClay JC, Soans R, Nemr R, Williams N, Courcoul — View Citation
Courcoulas A, Coley RY, Clark JM, McBride CL, Cirelli E, McTigue K, Arterburn D, Coleman KJ, Wellman R, Anau J, Toh S, Janning CD, Cook AJ, Williams N, Sturtevant JL, Horgan C, Tavakkoli A; PCORnet Bariatric Study Collaborative. Interventions and Operatio — View Citation
Inge TH, Coley RY, Bazzano LA, Xanthakos SA, McTigue K, Arterburn D, Williams N, Wellman R, Coleman KJ, Courcoulas A, Desai NK, Anau J, Pardee R, Toh S, Janning C, Cook A, Sturtevant J, Horgan C, Zebrick AJ, Michalsky M; PCORnet Bariatric Study Collaborat — View Citation
McTigue KM, Wellman R, Nauman E, Anau J, Coley RY, Odor A, Tice J, Coleman KJ, Courcoulas A, Pardee RE, Toh S, Janning CD, Williams N, Cook A, Sturtevant JL, Horgan C, Arterburn D; PCORnet Bariatric Study Collaborative. Comparing the 5-Year Diabetes Outco — View Citation
Toh S, Rasmussen-Torvik LJ, Harmata EE, Pardee R, Saizan R, Malanga E, Sturtevant JL, Horgan CE, Anau J, Janning CD, Wellman RD, Coley RY, Cook AJ, Courcoulas AP, Coleman KJ, Williams NA, McTigue KM, Arterburn D, McClay J; PCORnet Bariatric Surgery Collaborative. The National Patient-Centered Clinical Research Network (PCORnet) Bariatric Study Cohort: Rationale, Methods, and Baseline Characteristics. JMIR Res Protoc. 2017 Dec 5;6(12):e222. doi: 10.2196/resprot.8323. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Body Mass Index (BMI) | Change in Body Mass Index (BMI) | 1, 3, and 5 years after primary bariatric procedure | |
Primary | Diabetes Remission | Remission of diabetes after primary bariatric procedure. Defined as individual no longer using any diabetes medication for at least 3 months and hemoglobin A1c (HbA1c) <6.5% after 3 months off of diabetes medication. | 1, 3, and 5 years after primary bariatric procedure | |
Primary | Reoperation/Rehospitalization Rate | Reoperation: Any additional bariatric procedure and other procedures related to device removals, gastric revisions, abdominal or incisional hernia repair, laparoscopy or laparotomy, and percutaneous endoscopic gastrostomy tube placements.
Rehospitalization: Any inpatient hospitalization following surgery that is not associated with a delivery, miscarriage, or abortion procedure. |
1, 3, and 5 years after primary bariatric procedure | |
Secondary | Weight regain | At 3 and 5 years after primary bariatric procedure; estimated as percent regain from the maximum weight (in kg) loss in the first 2 years following bariatric surgery. | 3 and 5 years after primary bariatric procedure | |
Secondary | Diabetes relapse | Diabetes relapse defined as restarting diabetes medications or HbA1c >=6.5% | 1, 3 and 5 years after primary bariatric procedure | |
Secondary | Change in hemoglobin A1C (HbA1c) | Change in HbA1c measures. | 1, 3, and 5 years after primary bariatric procedure | |
Secondary | Mortality Rate | Any death during the study period | 1, 3, and 5 years after primary bariatric procedure | |
Secondary | Composite Adverse Event | Event is defined using criteria from the Longitudinal Assessment of Bariatric Surgery (LABS) study and includes death; venous thromboembolism; percutaneous, endoscopic, or operative subsequent intervention; and, failure to be discharged from the hospitalization where the bariatric surgery was performed | 30-days after primary bariatric procedure |
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