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Prediction of clinical outcome in achalasia patients underwent peroral endoscopic myotomy

Prediction of clinical outcome in achalasia patients underwent peroral endoscopic myotomy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0001824
Enrollment
100
Registered
2016-02-19
Start date
2016-01-23
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Bundang CHA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: achalasia patients treated by POEM

Exclusion criteria

Exclusion criteria: Exclusion criteria were uncontrolled cardiovascular disoders, pulmonary disorders, severe infections, psycotic disorders, and inability to communicate.

Design outcomes

Primary

MeasureTime frame
symptom relief for achalasia, age, sex, disease duration, achalasia type, length of myotomy, esophageal diameter

Secondary

MeasureTime frame
symptom recurrence for achalasia

Countries

Korea, Republic of

Contacts

Public ContactWeon Jin Ko

Bundang CHA General Hospital

wisred@naver.com

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026