The applicability of endoscopic hand-suturing method by using through-the-scope needle holder.

The applicability of endoscopic hand-suturing method by using through-the-scope needle holder. - The applicability of endoscopic hand-suturing method

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000031288

Enrollment

Registered

2018-02-13

Start date

2017-11-27

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Esophagus Achalasia etc

Interventions

Procedure by EHS

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who have received complete information about the study and are willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: Inability or unwillingness of patients to give written informed consent Judged unsuitable for this study by the physician

Design outcomes

Primary

Measure	Time frame
The efficacy of endoscopic hand suturing method at the next day, 2 months and 1 year after the operation.	—

Secondary

Measure	Time frame
Adverse events rate. Patients are evaluated by obtaining blood samples and X-rays after the operation(operation day and next day).	—

Countries

Japan

Contacts

Public ContactAkiko Toshimori

Showa University Koto Toyosu Hospital Digestive Disease Center

akikotoshimori@med.showa-u.ac.jp03-6204-6000

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026