Skip to content

Peroral endoscopic long and short myotomy for achalasia: a randomized, controlled, single center study

Peroral endoscopic long and short myotomy for achalasia: a randomized, controlled, single center study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014989
Enrollment
Unknown
Registered
2018-02-26
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-03-05

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

Conditions

achalasia

Interventions

long tunnel group:Peroral endoscopic building a 11cm tunnel
short tunnel group:Peroral endoscopic building a 6cm tunnel

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) Aged between 18 to 70 years; (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
Esophageal barium;Gastroesophageal reflux disease questionnaire scores;quality of life;Operative time;

Countries

China

Contacts

Public ContactDeliang Liu

the Second Xiangya Hospital of Central South University

liudeliang@medmail.com.cn+86 13974812392

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 25, 2026