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Clinical Trial of 3D Electronic Endoscopy

A Prospective Multi-center Clinical Trial to Assess the Safety and Effectiveness of 3D Electronic Endoscopy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026652
Enrollment
Unknown
Registered
2019-10-17
Start date
2019-10-17
Completion date
Unknown
Last updated
2019-10-21

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

Conditions

Patients requiring laparoscopic exploration or surgical treatment

Interventions

Experimental group:MicroPort 3D Electronic Endoscopy System
Control Group:Olympus EndoEYE FLEX 3D

Sponsors

Sir Run Run Shaw Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 to 80 years; 2. Patients requiring laparoscopic exploration or surgical treatment; 3. Willing to cooperate and complete all follow-up visits; 4. All subjects are required to give informed consent to the this study and sign informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Severe cardiovascular or circulatory diseases; 2. Paticipated other clinical trials in the last 3 months; 3. Unable to understand research's requirements or unable to complete all the follow-up visits; 4. Other conditions judged by the investigators.

Design outcomes

Primary

MeasureTime frame
Rate of Image Quality;—

Secondary

MeasureTime frame
Operation Time;Intraoperative Blood Loss;Indwelling Time of Drainage Tube;—

Countries

China

Contacts

Public ContactXiujun Cai

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine

cxjzu@hotmail.com+86 571 86006667

Outcome results

None listed

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