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Clinical verification test for disposable endoscopic injection needle

Clinical verification test for disposable endoscopic injection needle

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018573
Enrollment
Unknown
Registered
2018-09-25
Start date
2018-05-03
Completion date
Unknown
Last updated
2018-10-01

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

Conditions

Digestive tract polyps and early cancer

Interventions

Test group:Disposable endoscope needles produced by Changzhou Heraeus Minimally Invasive Medical Devices Co., Ltd.
Control group:Use disposable needle for injection of endoscopes by Olympus Medical Co., Ltd.

Sponsors

Southern Medical University, Nanfang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-75 years old, male or female; (2) diagnosed as having digestive tract polyps and early cancer by clinical examination Patients with a size <2 cm) who require endoscopic mucosal resection (EMR); (3) The patient agrees to participate in the trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) severe heart, brain, lung and other organ dysfunction, leading to intolerance of endoscopy Healer; (2) Patients with severe blood coagulation disorders; (3) pregnant or lactating women; (4) Patients who have taken anticoagulant drugs within one week; (5) The clinical trial judge judges that the patient is not suitable for the test; (6) Participated in other similar clinical trials within 3 months before the trial.

Design outcomes

Primary

MeasureTime frame
Injection success rate;

Secondary

MeasureTime frame
package;Appearance;Needle surface;

Countries

China

Contacts

Public ContactLiu Side

Nanfang Hospital,Southern Medical University

liuside2011@163.com+86 13900212459

Outcome results

None listed

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