Skip to main content
Clinical Trials/NCT06006338
NCT06006338
Recruiting
Phase 1

The Clinical Value of 3D Self-healing Elastic Liver Model for Surgical Training and Preoperative Planning: a Preliminary Study

Zhejiang Cancer Hospital1 site in 1 country5 target enrollmentStarted: September 15, 2023Last updated:
ConditionsLiver Cancer

Overview

Phase
Phase 1
Status
Recruiting
Enrollment
5
Locations
1
Primary Endpoint
R0 resection rate

Overview

Brief Summary

Comprehensive preoperative planning and real-time intraoperative guidance are essential prerequisites for achieving precise liver resection. In pursuit of this goal, the investigators have developed innovative 3D printed liver models utilizing a physically crosslinked self-healing elastomer created through the copolymerization of 4-acryloylmorpholine (ACMO) and methoxy poly (ethylene glycol) acrylate (mPEGA). These printed models exhibit exceptional healing capabilities, efficiently restoring their structure within minutes at room temperature, and rapidly recovering within moments after being incised.

Herein, the investigators aim to assess the viability of employing these 3D printed liver models as instrumental tools in designing the optimal surgical approach through an iterative trial-and-error methodology. Concurrently, the investigators aim to determine whether the integration of these 3D printed models into conventional methods (contrast-enhanced CT or MRI) can enhance the safety, ease, and efficiency of hepatic resection procedures.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Device Feasibility
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 18-80 years old;
  • Patients with a resectable tumor in the liver;
  • Eastern Cooperative Oncology Group Performance status score: 0;
  • Child-Pugh classification: A;
  • The Laboratory test results meet the following criteria and patients can tolerate surgery: Haemoglobin≥90g/L, Neutrophil count≥1.5×10⁹/L, Platelet count≥100×10⁹/L, Aspartate or alanine aminotransferase≤5 upper limits of normal(ULN), alkaline phosphatase≤2.5 ULN, Serum albumin≥30g/L, serum creatinine\<1.5 ULN, International normalized ratios(INR)≤2 or Prothrombin time(PT)exceed ULN≤6s, Creatinine clearance≥60 mL/min.

Exclusion Criteria

  • Patients with extra-hepatic metastasis;
  • Anti-cancer therapy or surgery such as radiotherapy, radiofrequency ablation in 28 days prior to the surgery;
  • Clinically significant bleeding or bleeding tendencies within 3 months prior to enrollment or on thrombolytic or anticoagulant therapy;
  • Severe lung disease (eg, acute lung disease, pulmonary fibrosis that affects lung function, interstitial lung disease), uncontrolled diabetes mellitus (fasting blood glucose ≥10 mmol/L);
  • There are other unsuitable candidates for clinical trials, such as mental illness or alcohol dependence.

Outcomes

Primary Outcomes

R0 resection rate

Time Frame: 10 days

The proportion of patients who achieved pathological negative surgical margin

Secondary Outcomes

  • Operation time(Immediately after the surgery.)
  • Blood loss(Immediately after the surgery.)
  • Injury of vital vascular structures(Immediately after the surgery.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yuhua Zhang, MD

Vice director of Hepatobiliary and Pancreatic Surgery, Zhejiang Cancer Hospital

Zhejiang Cancer Hospital

Study Sites (1)

Loading locations...

Similar Trials