Achalasia
Conditions
Interventions
control group:Per-oral endoscopic myotomy for the treatment of achalasia using a traditional reusable endoscope
Experimental group:Per-oral endoscopic myotomy for the treatment of achalasia using a single-use endoscope
Sponsors
Chinese PLA General Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1.Patients with achalasia who visited our hospital and required endoscopic treatment. All patients must voluntarily agree to participate after being fully informed of the study's content, potential benefits, and risks. 2.Anticoagulant medications such as aspirin have been discontinued for more than 1 week prior to endoscopic therapy; 3.Aged between 18-70 years old; 4.Give informed consent, volunteer to participate in this clinical study, and be able to cooperate in completing the questionnaire.
Exclusion criteria
Exclusion criteria: 1.Patients with contraindications to endoscopic treatment; 2.Pregnant and lactating women; 3.Minors 70 years of age.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse event; | — |
Secondary
| Measure | Time frame |
|---|---|
| Complications;Image clarity of disposable portable endoscopes;Operational performance of disposable portable endoscopes.; | — |
Countries
China
Contacts
Public ContactNingli Chai
Chinese PLA General Hospital
Outcome results
None listed