Bariatric Surgery for ESRD Patients vs Control

NCT ID: NCT00580762

Last Updated: 2016-09-07

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 5 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-10-31
• Study Completion Date: 2011-07-31

Brief Summary

This study will address a true clinical problem by developing a risk/benefit analysis for rapid surgical weight loss in the ESRD population. The risks of surgical intervention, as well as, potential nutritional concerns, balanced with that of the potential medical benefits associated with significant weight loss.

Detailed Description

The study will be designed to compare two cohorts of patients that will undergo laparoscopic RYGB. Cohort 1 will include ESRD patients on HD who meet the NIH guidelines and preoperative requirements for RYGB. Cohort 2 will include non-ESRD patients who meet the NIH guidelines and preoperative requirements for RYGB. Laparoscopic RYGB will be performed in ESRD patients who meet the guidelines recommended by the National Institutes of Health consensus statement . This includes patients who either have a BMI≥40 kg/m2 or have a BMI≥35 kg/m2 and have a significant morbidity attributed to their obesity (i.e. sleep apnea, hypertension, and diabetes mellitus). All patients will undergo a complete pre-operative evaluation inclusive of dietary instruction, assessment of surgical risk, psychosocial evaluation and compliance evaluation. This evaluation will be conducted through an existing infrastructure at the investigators Bariatric Surgery Center. Patients will be required to be on hemodialysis or able to be converted to hemodialysis for the perioperative period. All procedures will be performed by the same team of surgeons, experienced in both laparoscopic RYGB, organ transplantation and general surgery in ESRD patients. The risks involved with Roux-en-Y gastric bypass surgery will be discussed with the patient. These risks are inherent to the procedure, however the procedure is being conducted for medical appropriate reasons and therefore the benefits to the procedure outweigh the risks. At the present time, it is believed, without any justification, that this procedure is more risky or too risky in the ESRD population. A primary objective of this study is to investigate this question.

Conditions

Obesity; ESRD

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

ESRD

End-Stage Renal Disease (ESRD) patients on dialysis who meet the NIH guidelines and preoperative requirements for RYGB will undergo laparoscopic RYGB

Group Type: EXPERIMENTAL

Roux-en-y gastric bypass (RYGB)

Intervention Type: PROCEDURE

Non-ESRD

Non-ESRD patients who meet the NIH guidelines and preoperative requirements for RYGB will undergo laparoscopic RYGB

Group Type: ACTIVE_COMPARATOR

Roux-en-y gastric bypass (RYGB)

Intervention Type: PROCEDURE

Interventions

Roux-en-y gastric bypass (RYGB)

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Obese ESRD patients with a BMI≥ 40kg/m2 or ≥35kg/m2 with an medical complication attributed to morbid obesity (NIH guidelines).REF

2. Age ≥ 18 and ≤ 65

3. Patients must be on hemodialysis for one month.

4. Patients listed for kidney transplant in a UNOS certified kidney transplant center.

5. Patients have accrued less than 18 months of waiting time.

6. Completion of pre-RYGB psychosocial evaluation.

7. Completion of pre-RYGB dietary counseling.

8. Completion of pre-RYGB surgical risk assessment inclusive of cardiac evaluation.

9. Full reciprocal understanding of informed consent and the risks and benefits of RYGB procedure.

10. Acceptance of clinical protocol evaluations requiring scheduled clinic visits and laboratory blood draws.

Exclusion Criteria

1. Age < 18 and > 65.

2. Patients with a history of peritoneal dialysis related bacterial peritonitis.

3. Peritoneal dialysis patients not willing to undergoing temporary hemodialysis.

4. History of difficult vascular access as defined by the inability to obtain permanent upper extremity or temporary jugular venous access.

5. History of poor hemodialysis performance.

6. Patients enrolled in another study within 6 months of initiation.

7. Patients listed for kidney transplant in a different UNOS region that has shorter transplant waiting times than the region governing the investigators institution.

8. Patients unwilling to be made temporarily unavailable for transplant.

9. History of non-compliance with medical care.

10. Uncontrolled psychiatric illness (ie. depression, anxiety, attention deficit disorder (ADD), uncontrolled binge eating disorder)

11. Inability to provide reciprocal understanding of informed consent.

12. Failure to complete the preoperative work-up (psychosocial, dietary and surgical risk) for RYGB.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Yale University

OTHER

Sponsor Role: lead

Responsible Party

Sanjay Kulkarni

Director of Kidney Transplantation

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sanjay Kulkarni, MD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

Yale University School of Medicine

New Haven, Connecticut, United States

Countries

United States

Other Identifiers

0508000519

Identifier Type: -

Identifier Source: org_study_id