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Study on usefulness of jelly injection in hemostasis during endoscopic submucosa dissection

Study on usefulness of jelly injection in hemostasis during endoscopic submucosa dissection - JH trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038692
Enrollment
43
Registered
2019-12-24
Start date
2020-01-01
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

gastric cancer,esophageal cancer,colorectal tumor

Interventions

For bleeding during endoscopic submucosal dissection, an oral rehydration jelly is injected to identify the bleeding site. There is no upper limit to the number and amount of jelly injections. For ble

Sponsors

Department of Gastroenterology, Kanazawa University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who are scheduled for endoscopic submucosal dissection of the esophagus, stomach, and large intestine. 2) Age at the time of obtaining consent is 20 years old or older and less than 80 years old. 3) Informed consent has been obtained from the patient regarding participation in this study.

Exclusion criteria

Exclusion criteria: 1) Patients who are likely to have perforated or have perforated during endoscopic submucosal dissection.

Design outcomes

Primary

MeasureTime frame
In Phase I, OS-1 jelly was used to improve the field of view and evaluate safety when hemostasis occurred. In Phase II, the time taken to identify the bleeding site in the normal group and jelly combination group.

Countries

Japan

Contacts

Public ContactHajime Takatori

Kanazawa University Hospital Department of Gastroenterology

hajimetakatori@gmail.com0762652235

Outcome results

None listed

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