Robot-assisted percutaneous scaphoid fracture fixation versus traditional percutaneous scaphoid fracture fixation for scaphoid waist fracture: a prospective randomized controlled trial

A clinical pathway study for TiRobot assisted percutaneous carpal fracture fixation

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000035036

Enrollment

Unknown

Registered

2020-07-28

Start date

2021-06-01

Completion date

Unknown

Last updated

2020-08-03

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

Conditions

scaphoid waist fracture

Interventions

experimental group:Robot-assisted percutaneous scaphoid fracture fixation

control group:Traditional percutaneous scaphoid fracture fixation

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Willing to participate this trial and sign the consent form for surgery and trial; 3. Acute (within 2 weeks) non-displaced waist scaphoid fracture or the displacement of waist scaphoid fracture within 1mm.

Exclusion criteria

Exclusion criteria: 1. Severe trauma or arthritis to the study hand or wrist, for example: multiple carpal fractures; 2. The study wrist could not make full extension or flexion; 3. Patients with absolute or relative contraindication to the surgery; 4. Scaphoid fracture nonunion.

Design outcomes

Primary

Measure	Time frame
Accuracy of screw placement;	—

Secondary

Measure	Time frame
time of surgery;dose of radiation during surgery;the number of guide-wire attempts;PRWE scores;Grip strength and pinch strength;movement degress;pain score;	—

Countries

China

Contacts

Public ContactBo Liu

Beijing Ji-Shui-Tan Hospital

jstdrliubo@163.com+86 13911063662

Outcome results

None listed

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