Safety and Feasibility of Endomina, an Candy Cane Syndrome Endoluminal Suturing Device
Ключови думи
Резюме
Описание
Surgery is currently the only effective treatment for morbid obesity and can be divided into restrictive surgeries (Lap Band and Sleeve gastrectomy), malabsorptive surgeries (Biliary pancreatic deviation and duodenal switch) or a combination of both (RYGBP).
This latter technique is the most common and most effective surgical procedure performed worldwide and has been processed to be an effective treatment of morbid obesity and its complications, achieving excess weight loss of 65 to 80 %; 1-2 years after surgery (1,2).
Morbidity after RYGB includes the candy cane syndrome or afferent loop syndrome. Candy cane Roux syndrome in patients who have undergone RYGB refers to an excessively long blind afferent Roux limb at the gastrojejunostomy causing postprandial pain often relieved by vomiting. It is believed that the blind afferent limb ("candy cane") acts as an obstructed loop when filled with food (often preferentially), and the distention of the loop causes pain until the food either spills into the Roux limb or is vomited back out (3).
Patients have been reported presenting as early as three months and as late as 11 years after their initial RYGB, typically with symptoms of postprandial epigastric pain, nausea, vomiting, and reflux or food regurgitation (4). The diagnosis is confirmed by upper gastrointestinal contrast studies or endoscopy. On upper gastrointestinal series, the afferent limb fills before contrast spills into the Roux limb. On upper endoscopy, the afferent limb is usually the most direct outlet of the gastrojejunostomy (3).
The treatment is revision bariatric surgery, most commonly laparoscopic resection of the afferent limb, which ranged in length from 3 to 22 cm in one study (mean of 7.6 cm) (3). Symptoms resolve after revision surgery in most patients. Surgeons should minimize the length of the blind afferent loop left at the time of initial RYGB to prevent candy cane Roux syndrome.
Endomina (Endo Tools Therapeutics, Gosselies, Belgium) is a CE marked device that may be attached to an endoscope inside the body and allows remote actuation of the device during a peroral intervention. It offers the possibilities of making transoral full thickness tissue apposition and may allow performing, via a transoral route, large plications with tight serosa to serosa apposition.
Дати
Последна проверка: | 05/31/2020 |
Първо изпратено: | 06/14/2018 |
Очаквано записване подадено: | 07/23/2018 |
Първо публикувано: | 07/30/2018 |
Изпратена последна актуализация: | 06/28/2020 |
Последна актуализация публикувана: | 06/29/2020 |
Действителна начална дата на проучването: | 03/05/2018 |
Приблизителна дата на първично завършване: | 03/02/2020 |
Очаквана дата на завършване на проучването: | 03/02/2020 |
Състояние или заболяване
Интервенция / лечение
Device: Intervention
Фаза
Групи за ръце
Arm | Интервенция / лечение |
---|---|
Experimental: Intervention | Device: Intervention The jejunum between the two loops is sutered with Endomina and cut 15 days later. |
Критерии за допустимост
Възрасти, отговарящи на условията за проучване | 18 Years Да се 18 Years |
Полове, допустими за проучване | All |
Приема здрави доброволци | Да |
Критерии | Inclusion Criteria: 1. Proven Candy cane syndrome by barium swallow 2. Age between 18-65 years; 3. Must be able to comply with all study requirements for the duration of the study as outlined in the protocol. This includes complying with the visit schedule as well as study specific procedures such as: clinical assessment, endoscopy, radiography, as well as laboratory investigations; 4. Must be able to understand and be willing to provide written informed consent; 5. Must live within 75 km of the treatment site; 6. Had followed the bariatric multidisciplinary workup (blood analyses, dietician, psychologist and doctor appointments). Exclusion Criteria: 1. Achalasia and any other esophageal motility disorders; 2. Severe esophagitis; 3. Gastro-duodenal ulcer; 4. Severe renal, hepatic, pulmonary disease or cancer; 5. GI stenosis or obstruction; 6. Pregnancy, breastfeeding or willing to become pregnant in the coming 18 months; 7. Anticoagulant therapy; 8. Impending gastric surgery 60 days post intervention; 9. Currently participating in other study |
Резултат
Първични изходни мерки
1. Characterisation of safety by measurement of the incidence of all adverse device effects (ADE) [6 months]
Вторични изходни мерки
1. Efficacy of the device: Dakkak and Bennett dysphagia score [6 months]