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Resolution of Comorbidities & Safety and Efficacy of Greater Curvature Plication in Obese Patients

Primary Purpose

Morbid Obesity

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Laparoscopic Greater Curvature Plication
Sponsored by
Singh, Kuldeep, M.D., P.A.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Morbid Obesity

Eligibility Criteria

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

Inclusion Criteria:

  1. Subject is willing to give consent and comply with evaluation and treatment schedule
  2. 18 to 65 years of age
  3. Have a BMI > 30 with one or more significant co-morbid medical conditions which are generally expected to be improved, reversed, or resolved by weight loss. these conditions include but are not limited to:

    • Hyperlipidemia
    • Type 2 diabetes
    • Mild Obstructive Sleep Apnea
    • Hypertension
    • Osteoarthritis of the hip or knee
  4. Agree to refrain from any type of weight-loss drug ( prescription or OTC) or elective procedure that would affect body weight for the duration of the trial
  5. HbA1C < 11 %
  6. For subjects who have Type 2 Diabetes, the anti-diabetic medication regimen is no more complex than oral metformin plus one oral sulfonylurea plus once daily insulin injection.
  7. Ability to self-pay for the procedure and follow up.

Exclusion Criteria:

-

Sites / Locations

  • Saint Agnes HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Morbid Obese patients

Arm Description

This purpose of this study is to find out more about the safety and effectiveness of the Laparoscopic Greater Curvature Plication (LGCP) for Morbid Obese Patients with related problems such as diabetes, hypertension, high cholesterol, mild obstructive sleep apnea and joint problems.

Outcomes

Primary Outcome Measures

Percent excess weight loss

Secondary Outcome Measures

Resolution of Comorbidities
After one year, evaluate each patient to see if the patient has had resolution of any types of comorbidities they manifested pre op; diabetes, hypertension, high cholesterol, mild obstructive sleep apnea, and joint problems

Full Information

First Posted
December 9, 2014
Last Updated
December 17, 2014
Sponsor
Singh, Kuldeep, M.D., P.A.
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1. Study Identification

Unique Protocol Identification Number
NCT02315105
Brief Title
Resolution of Comorbidities & Safety and Efficacy of Greater Curvature Plication in Obese Patients
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
August 2011 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
August 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Singh, Kuldeep, M.D., P.A.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to find out more about the safety and effectiveness of the Laparoscopic Greater Curvature Plication (LGCP) procedure in patients with obesity and related problems such as diabetes, hypertension, high cholesterol, mild obstructive sleep apnea, and joint problems. LGCP is a less invasive weight loss surgery procedure than some of the other weight loss surgeries and it is possible that there are fewer risks with this procedure than with the other weight loss surgeries. LGCP is considered an experimental procedure and this study is being done to look at the long-term outcomes.
Detailed Description
LGCP is a procedure in which the stomach is folded inwards to that its capacity to hold amounts of food is decreased. This is done under general anesthesia. The operation takes about an hour and is done laparoscopically. Laparoscopic approach entails placing 4-5 small incisions in the abdomen around the umbilicus and filling the abdomen with CO2 through the small tubes called Trocars. this helps life the abdominal wall and create space so that the surgeon can carry out his/her work using long instruments with thickness similar to a regular lead pencil. The attachments of the stomach to the spleen are freed up and the outside is folded inside and stitched up to keep it from folding in. To ensure that the surgeon has not obstructed the passage in or out of the stomach, a tube is placed in the stomach at the time of the creation of the fold and checked again at the end of the procedure with a camera in the stomach which is placed through the mouth to ensure the desired outcome is achieved. At the conclusion of the procedure, the skin is closed with absorbable sutures and adhesive tapes are applied to the skin. The patient recovers in the recovery room for about an hour and a half prior to coming to their room in the hospital. The post operative visit will be up to 7 days after the procedure. During this visit, medical information will be obtained including information about medications. There will be follows 3-10 after the surgery. These visits may include: obtaining medical information about the patient, including the medical conditions and medications Checking the patient's weight Blood tests Endoscopic evaluation of the stomach if necessary. The timing of the visits is as follows: Visit 3: 1 month after surgery Visit 4: 3 months after surgery Visit 5: 6 months after surgery Visit 6: 12 months after surgery Visit 7: 18 months after surgery Visit 8: 24 months after surgery Visit 9: 30 months after surgery Visit 10: 36 months after surgery The study is three (3) years (36 months) including following up visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morbid Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
75 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Morbid Obese patients
Arm Type
Experimental
Arm Description
This purpose of this study is to find out more about the safety and effectiveness of the Laparoscopic Greater Curvature Plication (LGCP) for Morbid Obese Patients with related problems such as diabetes, hypertension, high cholesterol, mild obstructive sleep apnea and joint problems.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic Greater Curvature Plication
Intervention Description
LGCP is a procedure in which the stomach is folded inwards to that its capacity to hold amount of food is decreased dramatically. This is done under general anesthesia. The operation takes about 1 hour and is done laparoscopically. The attachments of the stomach to the spleen are feed up and the outside is folded inside and stitched up to keep it from folding in. To ensure that the surgeon has not obstructed the passage in or out of the stomach, a tube ( Bougie) is placed in the stomach at the time of the creation of the fold and checked again at the end of the procedure with a camera in the stomach which is placed through the mouth (EGD- upper endoscopy) to ensure the desired outcome is achieved.
Primary Outcome Measure Information:
Title
Percent excess weight loss
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Resolution of Comorbidities
Description
After one year, evaluate each patient to see if the patient has had resolution of any types of comorbidities they manifested pre op; diabetes, hypertension, high cholesterol, mild obstructive sleep apnea, and joint problems
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: Subject is willing to give consent and comply with evaluation and treatment schedule 18 to 65 years of age Have a BMI > 30 with one or more significant co-morbid medical conditions which are generally expected to be improved, reversed, or resolved by weight loss. these conditions include but are not limited to: Hyperlipidemia Type 2 diabetes Mild Obstructive Sleep Apnea Hypertension Osteoarthritis of the hip or knee Agree to refrain from any type of weight-loss drug ( prescription or OTC) or elective procedure that would affect body weight for the duration of the trial HbA1C < 11 % For subjects who have Type 2 Diabetes, the anti-diabetic medication regimen is no more complex than oral metformin plus one oral sulfonylurea plus once daily insulin injection. Ability to self-pay for the procedure and follow up. Exclusion Criteria: -
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kuldeep Singh, MD
Phone
3014902193
Email
dockds@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Nicole Sansbury, MPH
Phone
3014902193
Email
nsansbury@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kuldeep Singh, MD
Organizational Affiliation
Saint Agnes Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saint Agnes Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kuldeep Singh, MD
Phone
301-490-3736
Email
lapman21229@yahoo.com
First Name & Middle Initial & Last Name & Degree
Kuldeep Singh, MD

12. IPD Sharing Statement

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Resolution of Comorbidities & Safety and Efficacy of Greater Curvature Plication in Obese Patients

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