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Esophageal Achalasia clinical trials

View clinical trials related to Esophageal Achalasia.

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NCT ID: NCT03063463 Enrolling by invitation - Achalasia Clinical Trials

Mechanisms of Weight Loss in Patients Diagnosed With Achalasia

Start date: February 15, 2017
Phase:
Study type: Observational

Currently there are no existing data to determine why some achalasia patients lose weight while others do not. The purpose of this study is to gather data from patients diagnosed with achalasia to determine if differences may be identified between those who lose weight and those who do not that would help us better understand the mechanism of weight loss in this population.

NCT ID: NCT03012854 Recruiting - Clinical trials for Esophageal Achalasia

Different Surgical Procedures of Peroral Endoscopic Myotomy(POEM) for Esophageal Achalasia

Start date: December 2016
Phase: N/A
Study type: Interventional

This study compares the clinical efficacy of safety of circular myotomy and full-thickness myotomy guided by peroral endoscopic in treatment of incision length of ≤7cm and of ≥7cm in achalasia patients.

NCT ID: NCT02999451 Completed - Clinical trials for Esophageal Achalasia

Snare-assisted POEM for Treatment of Esophageal Achalasia

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

POEM is a new intervention for the treatment of achalasia and has been reported to relieve the dysphagia symptom effectively. Although the cost of POEM method is less than the method of Laparoscopic Heller Myotomy and Fundoplication, it is still of an economic burden for the patients with achalasia. In this trial, investigators plan to use snare to assist POEM procedure, to observe the safety, efficacy and cost-effectiveness of this method, compared with other knifes-assisted procedure.

NCT ID: NCT02989883 Recruiting - Achalasia Clinical Trials

Clinical Outcomes of Peroral Endoscopic Myotomy

Start date: October 2016
Phase: N/A
Study type: Interventional

Esophageal outflow obstruction is characterized by failure to relax the lower esophageal sphincter (LES), resulting in impaired flow of ingested food into the stomach. The subsequent stasis of ingested food leads to symptoms of dysphagia, regurgitation, chest pain, and weight loss. The core objective of the treatment of esophageal outflow obstruction is to disrupt the LES and reduce its pressure to allow esophageal emptying. Therapeutic options include pharmacologic therapy, Botulinum toxin injection, pneumatic balloon dilation, and surgical myotomy with partial fundoplication. In addition, peroral endoscopy myotomy (POEM) has recently been introduced as a minimally invasive treatment, but there have a few studies regarding long-term outcomes. The aim of this study is to evaluate clinical outcomes of POEM for esophageal outflow obstruction.

NCT ID: NCT02931565 Terminated - Achalasia Clinical Trials

Study of IW-1701, A Stimulator of Soluble Guanylate Cyclase (sGC), in Patients With Type I or II Achalasia

Start date: April 6, 2017
Phase: Phase 2
Study type: Interventional

The objectives of this study are as follows: In participants with primary Type I or II achalasia, following a single 5-mg dose of olinciguat (IW-1701), - To assess the safety and tolerability - To determine the effects on measures of esophageal function by high-resolution impedance manometry (HRIM) - To determine the pharmacokinetic (PK) parameters

NCT ID: NCT02773589 Completed - Esophagus Achalasia Clinical Trials

Prospective Evaluation of a New Approach to Perform an Esophageal Myotomy: the Transesophageal Submucosa Approach

Start date: March 2014
Phase: N/A
Study type: Interventional

Achalasia is an esophagus motor disability characterized by a lack of relaxation of the lower esophageal sphincter (LES) to deglutition. Myotomy is the gold standard surgical technique allowing to cure this pathology. In this study, investigators are using a new endoluminal technique of myotomy, innovative and less invasive, called POEM (PerOral Endoscopic Myotomy). This technique does not require any cutaneous incision. Mini-invasive surgery is more and more associated to endoscopy. The practice was initiated by the accession of natural orifice transluminal endoscopic surgery (NOTES). In this context, the introduction of the POEM technique seems to be an original approach and a natural evolution to a new generation of surgical endoscopy.

NCT ID: NCT02770859 Enrolling by invitation - Achalasia Clinical Trials

Per-Oral Endoscopic Myotomy (POEM) for the Treatment of Achalasia, Database Repository

POEM
Start date: October 16, 2014
Phase:
Study type: Observational [Patient Registry]

POEM (Per-Oral endoscopic myotomy (creating a muscle [esophagus] opening), an incision-less (no cutting of the surface of the body) endoscopic procedure, is an effective non-surgical alternative to release the muscle & sphincter of the LES for the treatment of achalasia.

NCT ID: NCT02663206 Withdrawn - Clinical trials for Esophageal Achalasia

Peroral Endoscopic Myotomy Versus Botulinum Toxin Injection in Spastic Esophageal Disorders

Start date: September 2016
Phase: N/A
Study type: Interventional

To compare the efficacy of peroral endoscopic myotomy and Botulinum toxin injection in spastic esophageal disorders.

NCT ID: NCT02606578 Terminated - Achalasia Clinical Trials

Achalasia Patient Reported Outcomes

Start date: October 2015
Phase:
Study type: Observational

Patients that are either scheduled to undergo or have undergone an achalasia procedure at the Mayo Clinic Rochester are asked to participate. The purpose of this study is to gather information and determine if one of these procedures is superior to the other.

NCT ID: NCT02572193 Recruiting - Clinical trials for Esophageal Achalasia

To Assess the Feasibility of Same Day Discharge Following a POEM Procedure

POEM2
Start date: October 2015
Phase: N/A
Study type: Interventional

This is a study of an investigational surgical procedure for the treatment of achalasia the inability of smooth muscle to move food down the esophagus. A new procedure, called the POEM procedure (per oral endoscopic myotomy) has been developed for achalasia. This study is being performed to determine if patients can go home on the same day as their procedure.