Comparative Study of Per-oral Endoscopic Myotomy (POEM) in Treatment - naïve Achalasia Patients Versus Patients With Previous Pneumatic Dilation
NCT07287787
Achalasia, Esophageal, Deglutition Disorders
View Trial DetailsNCT Number: NCT07334639
This goal of the study is to assess the effect of weight gain in patients with achalasia after they are treated. The main question to be answered is if weight gain after achalasia treatment is associated with worsening metabolic status. Patients will be compared between their baseline status at the time of treatment and 1 year after treatment. Participants will have metabolic tests performed at these 2 times including blood tests.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Hadassah Medical Center, Jerusalem, Israel
Background Achalasia is a disease characterized by the loss of the myenteric neurons that coordinate esophageal peristalsis and lower esophageal sphincter (LES) relaxation.1 As a result, there is aperistalsis of the esophagus and impaired LES relaxation after deglutition. The primary symptoms are dysphagia, regurgitation, and chest pain.
Weight loss is also common.2 Studies have shown weight loss occurring in between 35-69% of achalasia patients.3,4 One study reported that patients with Type II Achalasia were more likely to have weight loss than the other subtypes.5 Studies have also shown that patients with achalasia, even when not underweight, are at risk of malnutrition.6 Recently, studies have begun assessing the weight gain that occurs after successful treatment of achalasia.7-10 These studies have evaluated achalasia patients after laparoscopic Heller myotomy (LHM),7 peroral endoscopic myotomy (POEM),8,9 or a combination of treatment modalities.10 They have consistently shown significant weight gain after treatment, with many patients becoming overweight or obese.
However, the impact of this weight gain has not been objectively evaluated. Thus, to our knowledge, no studies have evaluated the cardiovascular or metabolic effects of this post-treatment weight gain.
Goals Therefore, we aim to evaluate the metabolic effects of post-treatment weight gain in in a cohort of achalasia patients undergoing treatment by assessing the relationship between weight gain and glycemic control, cholesterol levels, blood pressure, and hepatic steatosis.
Methods A prospective pilot study will be performed at both Shamir Medical Center and Hadassah Medical Center. All adult patients diagnosed with achalasia and undergoing either POEM or LHM for treatment of achalasia will be included.
The cases of achalasia will be reviewed thoroughly for demographic, clinical, laboratory, and manometric information.
Additionally, prior to POEM, the patient will be evaluated for:
Statistical analyses Each patient's follow-up results will be compared to their pre-treatment results. Outcomes will include changes in levels of hepatic steatosis, waist circumference, body fat percentage, fasting glucose, Hgb A1c, cholesterol, liver function tests, and triglycerides compared to baseline, and the relationship in these changes to any weight gained. The primary outcome will be the change in hepatic steatosis on Fibroscan testing.
Continuous variables with a normal distribution will be reported as mean with standard deviation (SD), while those with a skewed distribution will be reported as median with interquartile range (IQR). Comparisons of categorical variables will be performed using the Chi-square test and Fisher's Exact test. Comparisons involving continuous variables will be performed using the Mann-Whitney U test. For all statistical calculations, a p-value <0.05 will be considered statistically significant.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 1 year
The degree of hepatic steatosis assessed on FibroScan at baseline compared to 1 year later
Time frame: 1 year
Change in fasting glucose between baseline and 1 year later
Time frame: 1 year
Change in Hgb A1c level between baseline and 1 year later
Time frame: 1 year
Change in cholesterol between baseline and 1 year later
Time frame: 1 year
Change in triglycerides between baseline and 1 year later
Time frame: 1 year
Change in weight between baseline and 1 year later
Time frame: 1 year
Change in waist circumference between baseline and 1 year later
Time frame: 1 year
Change in body fat percentage between baseline and 1 year later
Time frame: 1 year
Change in liver function tests between baseline and 1 year later
Time frame: 1 year
Change in resting blood pressure between baseline and 1 year later. Both the systolic and diastolic values will be assessed.
Time frame: 1 year
Change in Eckhardt score between baseline and 1 year later. The Eckhardt score goes from 0 to 12 with higher numbers meaning more severe symptoms.
Contact information is provided by the study sponsor or research team.
Assaf-Harofeh Medical Center
Other Gov
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