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Evaluating the Efficacy and Results of Endoscopic Gastroplasty Performed Using Overstitch in Patients With Obesity.

Primary Purpose

Obesity

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Endoscopic gastroplasty
Sponsored by
Kaiser Clinic and Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • BMI > 30 and < 36 with or without comorbidities
  • BMI > 36 and < 40 without comorbidities

Exclusion Criteria:

  • Prior gastric surgery
  • Use of anticoagulants
  • Psychiatric disorders
  • Severe esophagitis

Sites / Locations

  • Mario Covas Hospital
  • Kaiser Day hospital
  • 9 de Julho Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Endoscopic gastroplasty

Arm Description

Make a gastric tube similar to that obtained in surgical gastroplication however it will be created using intragastric endoscopic sutures.

Outcomes

Primary Outcome Measures

Weight loss
Weight in Kg and Body Mass Index (BMI) in kilograms by meters squared

Secondary Outcome Measures

Blood count
Measured in cmm
Hb1AC
Measured in percentage
Cholesterol
Measured in mg/dL
Fasting blood glucose
Measured in mg/dL
Procedural complications
Complications related to the procedure, either at the time of the procedure (bleeding, perforation and suture rupture) or in the postoperative period, performing an endoscopy at 6 months and 1 year to evaluate the suture line.

Full Information

First Posted
March 6, 2017
Last Updated
August 16, 2022
Sponsor
Kaiser Clinic and Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03088332
Brief Title
Evaluating the Efficacy and Results of Endoscopic Gastroplasty Performed Using Overstitch in Patients With Obesity.
Official Title
Prospective Multicenter Study to Evaluate the Efficacy and Results of Endoscopic Gastroplasty Performed Using Overstitch in Patients With Class I and II Obesity.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Clinic and Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Obesity is a chronic disease that has grown to epidemic characteristics in Brazil and around the world in recent years. Treatment for patients with class III or class II obesity with comorbidities is already well established, with bariatric surgery being the best option. However, there is no consensus as to the best treatment for cases of class I and class II obesity without comorbidities. The objective of this research will be to make a gastric tube similar to that obtained in surgical gastroplication however it will be created using intragastric endoscopic sutures. The procedures will be performed at the Endoscopy Service of the Mario Covas Hospital in São Paulo, SP. Data collection will be performed at the same location.
Detailed Description
The objective of this research will be to make a gastric tube similar to that obtained in surgical gastroplication however it will be created using intragastric endoscopic sutures. The secondary objective will be to correlate demographic, endoscopic and laboratory data with the results of this procedure. Patients and Methods: Patients with class I obesity with or without comorbidities and patients with class II obesity without comorbidities, irrespective of gender and ethnic background, from the state of São Paulo and other states of the country will be submitted to vertical endoscopic gastroplasty. The procedures will be performed at the Endoscopy Service of the Mario Covas Hospital in São Paulo, SP. Data collection will be performed at the same location. Information will be obtained during the outpatient follow-up at the Hospital Mario Covas including demographic (gender, age), clinical (height, weight, time after procedure, systemic arterial hypertension, diabetes, dyslipidemia, smoking, alcohol consumption) and operative data (complications). Preparation for the procedure: All the exams will be performed at the Hospital Mario Covas after the patients have fasted for at least 8 hours. The procedure will begin with the patient in left lateral decubitus under general anesthesia performed by an anesthesiologist. Endoscopic sutures will be performed using 2-0 prolene thread until a tubular-shaped stomach is formed similar to a vertical gastrectomy. Recovery after the procedure: After the procedure and recovery from anesthesia, all patients will be discharged but only together with a companion. All patients will receive guidance and will remain in touch with a physician to report any adverse signs or symptoms. Outcomes Primary outcome: To confirm the efficacy of endoscopic sutures in the primary treatment of obesity. Secondary outcome: To evaluate the use of the endoscopic sutures in relation to demographic data.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
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
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Endoscopic gastroplasty
Arm Type
Experimental
Arm Description
Make a gastric tube similar to that obtained in surgical gastroplication however it will be created using intragastric endoscopic sutures.
Intervention Type
Procedure
Intervention Name(s)
Endoscopic gastroplasty
Intervention Description
Vertical endoscopic gastroplasty
Primary Outcome Measure Information:
Title
Weight loss
Description
Weight in Kg and Body Mass Index (BMI) in kilograms by meters squared
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
Blood count
Description
Measured in cmm
Time Frame
48 weeks
Title
Hb1AC
Description
Measured in percentage
Time Frame
48 weeks
Title
Cholesterol
Description
Measured in mg/dL
Time Frame
48 weeks
Title
Fasting blood glucose
Description
Measured in mg/dL
Time Frame
48 weeks
Title
Procedural complications
Description
Complications related to the procedure, either at the time of the procedure (bleeding, perforation and suture rupture) or in the postoperative period, performing an endoscopy at 6 months and 1 year to evaluate the suture line.
Time Frame
At the time of procedure and at 6 months and 1 year follow-up period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: BMI > 30 and < 36 with or without comorbidities BMI > 36 and < 40 without comorbidities Exclusion Criteria: Prior gastric surgery Use of anticoagulants Psychiatric disorders Severe esophagitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luiz Guatavo de Quadros, MD
Organizational Affiliation
Kaiser Clinica and Day Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mario Covas Hospital
City
Santo André
State/Province
SP
ZIP/Postal Code
09190-615
Country
Brazil
Facility Name
Kaiser Day hospital
City
Sao Jose do Rio Preto
State/Province
SP
Country
Brazil
Facility Name
9 de Julho Hospital
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
01409-002
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Evaluating the Efficacy and Results of Endoscopic Gastroplasty Performed Using Overstitch in Patients With Obesity.

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