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ObesityNCT03094936

Clinical Trial for Weight Regain Post-RYGB: APC Versus APC Plus Endoscopic Suture Technique

A study testing APC and Endoscopic Suture Technique (OverStitch TM) in people with Obesity, run by University of Sao Paulo General Hospital at 1 site in Brazil.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Obesity is a worldwide health and sociopolitical problem. Excessive body-weight currently affects over 50% of the Brazilian population. It has been well established that obesity is an independent health risk. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Obesity
What is being tested?
APC and Endoscopic Suture Technique (OverStitch TM)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteBrazil
Study dates
Apr 2017to Oct 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Subject has stoma dilation defined as greater than 12mm, assessed with an esophagogastroduodenoscopy performed pre-operatively
  • Subject is ≥ 18 yrs. of age and ≤ 60 yrs. of age
  • Subject has a BMI of > 30
  • Subject has history of obesity for > 2 yrs
  • Subject has had no significant weight change (<5% of total body weight) in last 6 months
  • Subject must have failed standard obesity therapy (diet, exercise, behavior modification, and pharmacologic agents either alone or in combination), which will be assessed through an interview performed by a team member of the study at baseline
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  • Subject is a reasonable candidate for general anesthesia
  • Subject agrees not to have any additional weight loss surgery or reconstructive surgery that may affect body weight (i.e. mammoplasty, liposuction, lipoplasty, etc) during the trial
  • Subject must be willing and able to participate in all aspects of the study and agree to comply with all study requirements for the duration of the study. This includes availability of reliable transportation and sufficient time to attend all follow-up visits.
  • Subject must be able to fully understand and be willing to sign the informed consent.

Who cannot join

  • Subject has had significant weight loss in the last 3 months, or between baseline and the study procedure
  • Mallampati (intubation) score greater than 3
  • Subject is observed during esophagogastroduodenoscopy to have heavily scarred, malignant or poor quality/friable tissue in areas of the stomach where sutures are to be placed
  • Subject has history of inflammatory disease of GI tract
  • Subject has a history of intestinal strictures or adhesions
  • Subject has renal and/or hepatic insufficiency
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  • Subject has chronic pancreatic disease
  • Subject has history of/or signs and/or symptoms of gastro-duodenal ulcer disease and/or active peptic ulcer
  • Subject has significant esophageal disease including Zenker's diverticulum, grade 3-4 reflux esophagitis, stricture, Barrett's esophagus, esophageal cancer, esophageal diverticulum, dysphagia, achalasia, or symptoms of dysmotility
  • Subject has a history of any significant abdominal surgery
  • Subject has had previous bariatric, gastric or esophageal surgery; intestinal obstruction; portal gastropathy; gastrointestinal tumors; esophageal or gastric varices, or gastroparesis
  • Subject has a hiatal hernia > 2cm
  • Subject has chronic/acute upper GI bleeding conditions
  • Subject has severe coagulopathy (prothrombin time > 3 seconds over control or platelet count < 100,000) or is presently taking heparin, coumadin, warfarin, or other anticoagulants or other medications which impede coagulation or platelet aggregation, if they cannot be ceased for the procedure
  • Female subject is of childbearing age and not practicing effective birth control, is pregnant or is lactating
  • Subject has symptomatic congestive heart failure, cardiac arrhythmia or unstable coronary artery disease.
  • Subject has cancer or life expectancy of < 2 yrs

Trial locations and contacts

1 site in 1 country.

Vitor O Brunaldi, MD contact

55-11-26617579

vbrunaldi@gmail.com

Brazil1 site, 1 recruiting
  • Hospital das Clinicas da Faculdade de Medicina da USP

    São Paulo, São Paulo, 05403-000

    Vitor O Brunaldi, MD, 1126616467, vitor.brunaldi@usp.br

    Eduardo GH de Moura, PhD, 1126616467, eduardoghdemoura@gmail.com

    Recruiting

Other trials in Brazil

About this study

Official title: Randomized Clinical Trial for Weight Regain Post-RYGB:Argon Plasma Coagulation Versus Argon Plasma Coagulation Plus Endoscopic Suture Technique

Obesity is a worldwide health and sociopolitical problem. Excessive body-weight currently affects over 50% of the Brazilian population. It has been well established that obesity is an independent health risk. Obese individuals are at increased to extremely high risk for many diseases and for early death relative to those with normal weights and waist circumferences. The increased disease susceptibility for this subset of patients includes hypertension, stroke, hyperlipidemia, sleep apnea, Type 2 diabetes, neoplasms, Gastro-Esophageal Reflux Disease, and musculoskeletal disorders.

Bariatric surgery is the most effective treatment for obesity. As bariatrics grow, the number of patients suffering from surgical-related complications also grows. One of the most worrisome long-term complications is weight regain, once the patient may be again affected by overweight-related comorbidities and face again pre-operative esthetic issues.

This trial focus on testing efficacy and safety of two endoscopic revisional procedures in patients suffering from weight regain following Roux-en-Y Gastric Bypass: Ablation with Argon Plasma Coagulation (APC) versus APC plus Endoscopic Full-thickness Suture (with Apollo Overstitch device). Pouch volume, gastric emptying and gut hormones changes will also be assessed.

Read the detailed description

Obesity is a worldwide health and sociopolitical issue. Excessive body-weight currently affects over 50% of the Brazilian population and around 13% of all world population. It has been well established that obesity is an independent risk factor. Obese individuals are at increased risk of diseases and earlier death compared to those with normal weight and waist circumferences. The increased disease susceptibility of this subset of patients includes hypertension, stroke, hyperlipidemia, sleep apnea, Type 2 diabetes, neoplasms, GERD, and musculoskeletal disorders.

Obese patients and their physicians have increasingly turned to surgery to solve the excess weight issue and the frequent co-morbid conditions that impact their health and quality of life. Roux-en-Y Gastric Bypass (RYGB) and Laparoscopic Gastric Banding (LGB) comprise around 70% of all weight loss procedures performed every year. They induce significant and perennial weight loss and reduce or eliminate associated co-morbid diseases, including Type 2 diabetes. Despite improvements in postoperative morbidity and mortality rates over the years, (in part due to the use of a laparoscopic approach), these procedures still carry significant risk. Recent studies have shown mortality rates with RYGB as high as 1.9%, and complications associated with LGB as high as 13%. Nonetheless, a secondary bariatric procedure due to weight regain carries significant complication rates and worse outcomes, compared to the primary procedure. Consequently, less invasive techniques are needed to reduce such risks.

Gastric restriction is an important principle of both RYGB and LGB. The OverStitchTM Endoscopic Suturing System (Apollo Endosurgery, Inc. Austin, Texas) is an approved device designed to endoscopic placement of suture(s) and approximation of soft tissue. This system offers the assistant doctor the ability to restrict gastric pouch size by approximating tissue endoluminally through an incisionless (per-oral) approach. The use of this system has the potential to reduce the complications associated with the current surgical approach but still reaching the desired gastric restriction. The OverStitch has safely been used clinically for a great number of procedures that demanded an incisionless or minimally invasive approach, including endoluminal revisions for post-bypass gastric stoma and/or pouch dilatation, post-bypass fistulae repair, and oversewing of marginal ulcers.

Besides this suturing device, other endoscopic methods have already been used to reduce dilated stoma. Among them, ablation with argon plasma coagulation (APC) is one of the most important since this device is worldly available and presents an acceptable cost. Recent studies associate APC prior to endoscopic suture and initial evidence supports superiority of this association.

However, literature is still lacking of studies to support the use of APC associated with endoscopic suturing instead of APC alone. Therefore, the main focus of this study is to directly compare short and long-term effectiveness and safety of APC versus APC plus Endoscopic Full-thickness suture with OverStitch device in patients suffering from weight regain following RYGB.

Moreover, gut hormones regulation regarding bariatric and revisional procedures have been studied recently and evidence suggests that hormonal changes may be an important factor in weight loss. Three of the most important gut hormones regarding weight balance are ghrelin, GLP1 and peptide YY. Ghrelin is known as hunger hormone. It is produced by cells in gastric fundus. Glucagon-like Peptide 1 (GLP1) and Peptide YY (PYY) are both hormones that regulate satiety and are produced by L cells along distal intestine. Evidence in bariatric show that after long-term ghrelin levels diminish while GLP and PYY reach higher post-prandial peak. Regarding revisional endoscopic therapy, gut hormone changes have never been studied. That is also focus of this study as secondary outcome.

Conditions
Obesity
Being tested
APC, Endoscopic Suture Technique (OverStitch TM)
Medical subject headings
Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • APCProcedure or surgery

    Ablation of the dilated gastro-jejunal anastomosis with Argon Plasma Coagulation. This procedure induces cicatrization process around the stoma and propitiates its reduction.

  • Endoscopic Suture Technique (OverStitch TM)Device

    Also called Apollo Overstitch

    OverStitchTM Endoscopic Suturing System. Stitches will be placed per-orally with the aforementioned device around the dilated stoma in order to reduce the diameter of the anastomosis. In this group, ablation with APC will be done immediately before suturing.

Study groups in NCT03094936
Study groupRoleWhat they receive
Group AOtherThis group own twenty patients who met all the inclusion criteria. These will be treated with APC.
Receives: Procedure: APC
Group BActive comparatorThis group own twenty patients who met all the inclusion criteria. These will be treated with APC plus Endoscopic Suture Technique (OverStitch TM).
Receives: Procedure: APC; Device: Endoscopic Suture Technique (OverStitch TM)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Absolute Weight Loss

    Absolute Weight Loss will be assessed through subtraction of the pre-operative weight and the weight at follow-up, and will be measured in kilograms (kgs).

    Measured: This outcome will be assessed at 12 months after the procedure

  2. Excess Weight Loss

    Excess Weight Loss will be assessed through calculation of the percentage of the overweight lost after the procedure at follow-up. Excess Weight is defined as the weight over BMI of 25 for each patient. Excess Weight Loss will be expressed as percentage (%).

    Measured: This outcome will be assessed at 12 months after the procedure

  3. Abdominal Circumference Reduction

    Subtraction between baseline abdominal circumference and this measure at follow-up. This outcome will expressed in centimeters (cm).

    Measured: This outcome will be assessed at 12 months after the procedure

  4. BMI reduction

    Subtraction between baseline BMI and this measure at follow-up. This outcome will expressed in kg/m2.

    Measured: This outcome will be assessed at 12 months after the procedure.

  5. Diabetes improvement

    This outcome will be assessed through a glucose tolerance test performed at baseline and another one performed at 1 year follow-up.

    Measured: This outcome will be assessed at baseline and 12 months after the procedure.

Secondary outcomes (6)
  1. Occurrence of Adverse Events

    Adverse events such as perforation, bleeding, pain, stenosis, vomiting, need of surgery.

    Measured: This outcome will be assessed continually after the procedure.

  2. Quality of Life Improvement

    This outcome will be assessed with SF-36 questionnaire.

    Measured: This outcome will be assessed at baseline and at 12 months.

  3. Eating Habits Evaluation

    This outcome will evaluate if there is any change in eating habits with TFEQ-R21 questionnaire

    Measured: This outcome will be assessed at baseline and at 12 months.

  4. Gut Hormones Response

    This outcome will evaluate at fasting, 30, 60, 90 and 120 minutes post-prandial the hormonal variation regarding Ghrelin, GLP1 and PYY

    Measured: This outcome will be assessed at baseline and at 12 months.

  5. Gastric (Pouch) Emptying

    This outcome will evaluate retention rate through scintigraphy.

    Measured: This outcome will be assessed at baseline and at 12 months.

  6. CT Volumetry of the Gastric Pouch

    This outcome will evaluate volumetry of the pouch before and 12 months after procedure through tridimensional computed tomography.

    Measured: This outcome will be assessed at baseline and at 12 months.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Mar 2017
  2. Study startApr 2017 (estimated)
  3. Primary completionSep 2018 (estimated)
  4. Study completionOct 2018 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03094936
Sponsor's protocol ID
43405415000000068
Status last verified
Mar 2017
First submitted
3 Sep 2015
Last updated
29 Mar 2017
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Publications

  • Brunaldi VO, Farias GFA, de Rezende DT, Cairo-Nunes G, Riccioppo D, de Moura DTH, Santo MA, de Moura EGH. Argon plasma coagulation alone versus argon plasma coagulation plus full-thickness endoscopic suturing to treat weight regain after Roux-en-Y gastric bypass: a prospective randomized trial (with videos). Gastrointest Endosc. 2020 Jul;92(1):97-107.e5. doi: 10.1016/j.gie.2020.03.3757. Epub 2020 Mar 23.

    PubMed 32217111

Questions about this trial

What is this clinical trial studying?

A study testing APC and Endoscopic Suture Technique (OverStitch TM) in people with Obesity, run by University of Sao Paulo General Hospital at 1 site in Brazil.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 29 Mar 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Ana C Cândido (55-11-26619577, ana.candido@hc.fm.usp.br), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Absolute Weight Loss (time frame: This outcome will be assessed at 12 months after the procedure). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03094936, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Mar 2017.

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