Dysphagia Clinical Trial
Official title:
Laparoscopy Heller Myotomy With Fundoplication Associated Versus Peroral Endoscopic Myotomy (POEM)
Verified date | April 2017 |
Source | University of Sao Paulo General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Achalasia is a disorder benign esophageal motor, which is characterized by failure to relax
the lower esophageal sphincter ( LES) in response to swallowing associated with lack of
peristalsis of the esophageal body. Its most common clinical presentation is dysphagia , and
occasionally chest pain , regurgitation , aspiration pneumonia and weight loss , resulting
in a large impact on daily activities and quality of life of affected individuals .
There is currently considered curative treatment for achalasia , dysphagia relief being the
primary therapeutic target and is forced to relax the LES by endoscopy or surgery. Thus ,
the most commonly used endoscopic treatments are forced dilatation of the cardia and
botulinum toxin. Laparoscopic Heller myotomy with antireflux procedure with therapy is
considered "gold standard " because of excellent results and minimal invasiveness. Currently
, pneumatic dilation and surgical treatment with the Heller myotomy with fundoplication are
strongly associated with the best therapeutic options available .
In recent years, the possibility of using endoluminal access in the treatment of achalasia
patients through the technique originally described as Natural orifices Translumenal
Endoscopic Surgery ( NOTES) and continuing advances in the submucosal dissection has enabled
the concomitant development of a new approach described as perioral endoscopic myotomy . In
2007, Pasricha et al , described the feasibility of endoscopic esophageal myotomy through a
submucosal tunnel initially in an animal model . The first performance of this procedure in
humans was described by Inoue et al , in 2010 , introducing the concept of transluminal
endoscopic surgery through natural orifices , with the objective of minimizing the trauma
and all the stress resulting from open surgical procedure . These authors call the procedure
as POEM ( Per Oral Endoscopic myotomy ) .
Status | Active, not recruiting |
Enrollment | 30 |
Est. completion date | December 2017 |
Est. primary completion date | November 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Patients between 18 and 70 years diagnosed with symptomatic achalasia (dysphagia score = II and Eckardt> 3) all grades including Rezende classification and Chicago Classification. - Patients who agree to participate in the study and signed an informed consent. Exclusion Criteria: - Treatment (s) prior (s) achalasia. - Patients with a history of esophageal, mediastinal and / or gastric surgery (except for gastric perforation). - Patients with liver cirrhosis and / or esophageal varices, Barrett's esophagus, esophageal stricture, premalignant or malignant esophageal lesions and coagulopathy. - Patients with severe cardiopulmonary disease or other serious illness that results in a high surgical risk. - Patients diagnosed with pseudoachalasia - Patients diagnosed with diverticulum in the distal esophagus. - Pregnancy and lactation. |
Country | Name | City | State |
---|---|---|---|
Brazil | Hospital das Clínicas da FMUSP | São Paulo | SP |
Lead Sponsor | Collaborator |
---|---|
University of Sao Paulo General Hospital |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Remission of symptoms dysphagia. | Patient selection will last for six months after the beginning of the study. Six months later, conduct additional examinations and randomization. Twelve months after the start of the project will be the completion of endoscopic surgery or laparoscopic surgery for resolution of dysphagia. The measure is a composite. | 12 months after the procedure performed. | |
Secondary | Running time of the procedure and hospitalization. | New outpatient medical visits for clinical reassessment, more precisely 30 days, 3 months, 6 months and 12 months after the procedure will be scheduled to measure the execution time of the procedure and hospitalization. The measure is a composite. | Starts 12 months after procedure performed. |
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