Clinical study on the application of digital imaging technology and 3D printing to improve the therapeutic effect of hernia support

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000034173

Enrollment

Unknown

Registered

2020-06-27

Start date

2020-08-01

Completion date

Unknown

Last updated

2020-06-29

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

Conditions

hernia

Interventions

Group 1:3D printing of hernia bracket

Group 2:hernia support

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Standard of hernia patients: patients aged 20-75 years who can't tolerate anesthesia and operation due to serious basic diseases or who can't perform hernia operation temporarily due to improper time and other reasons. In addition, there was no incarceration and necrosis of hernias and no symptoms and signs of intestinal obstruction. All subjects or their guardians must sign the informed consent before entering the trial.

Exclusion criteria

Exclusion criteria: The patient's health and personal condition can be treated by hernia operation. The contents of hernia include incarceration, necrosis, symptoms and signs of intestinal obstruction, poor personal compliance, and severe skin infection in the gastrofemoral area.

Design outcomes

Primary

Measure	Time frame
Herniation or not;	—

Secondary

Measure	Time frame
comfort level score;	—

Countries

China

Contacts

Public ContactJiazeng Xia

Wuxi Second People's Hospital

jiazengxiawuxi@njmu.edu.cn+86 13506187399

Outcome results

None listed

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