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Peroral endoscopic anterior and right-posterior myotomy for achalasia: a randomized, controlled, single center study

Peroral endoscopic anterior and right-posterior myotomy for achalasia: a randomized, controlled, single center study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15007211
Enrollment
Unknown
Registered
2015-10-14
Start date
2015-11-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

achalasia

Interventions

Anterior Group:Peroral endoscopic anterior myotomy
Right-posterior Group:Peroral endoscopic right-posterior myotomy

Sponsors

the Second XiangYa Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) The diagnosis of achalasia patients was made on the basis of clinical symptoms, barium esophaography, esophagogastroduodenoscopy (EGD) and high resolution manometry (HRM); (2) Eckardt score >=4; (3) Age between 18 to 70; (4) Without previous endoscopic or surgical treatment fro achalasia; (5) Non-sigmoid-type achalasia; (6)Patient consented to receive POEM at our hospital and signed an infromed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with severe coagulopathy (INR >2,Platelet 2 cm); (6) Other contradicitons of endoscopic examination and therapy, such as severe scoliosis, mental diseases, etc.

Design outcomes

Primary

MeasureTime frame
Eckardt Score;Esophageal high resolution manometry;complication;24 h PH testing;

Secondary

MeasureTime frame
quality of life;Operative time;Esophageal barium;Gastroesophageal reflux disease questionnaire scores;

Countries

China

Contacts

Public ContactDeliang Liu
liudeliang@memdmail.com.cn+86 13974812392

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 7, 2026