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Effectiveness Evaluation of Smart Closed Reduction Navigation Robot for Pelvic Fractures

Effectiveness Evaluation of Smart Closed Reduction Navigation Robot for Pelvic Fractures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128106
Enrollment
Unknown
Registered
2026-07-14
Start date
2026-07-15
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Pelvic Fracture

Interventions

Experimental group:Robotic System-Assisted Surgery

Sponsors

The Fourth Medical Center of the Chinese People's Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age: 18 years or older, regardless of gender; 2. Diagnosed with pelvic fractures of AO/OTA type 61-A, 61-B, or 61-C through imaging examinations (X-ray, CT), requiring surgical reduction and internal fixation; 3. Time from injury to planned surgery within 3 weeks; 4. The subject voluntarily agrees to participate in this study, can understand the study requirements, and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Expected unstable vital signs, unable to tolerate surgery expected to last more than 2 hours; 2. Allergy to implant materials (titanium alloy); 3. Serious underlying diseases (such as uncontrolled diabetes, severe cardiovascular or cerebrovascular diseases, coagulation disorders, etc.) expected to make surgery intolerable or affect postoperative assessment; 4. Cognitive dysfunction, history of mental illness, or any other reasons preventing cooperation with the study and follow-up; 5. Pregnant or breastfeeding women; 6. Participation in other interventional clinical studies within the past three months; 7. Pathological fractures or concurrent malignant tumors; 8. Active infection in the surgical area; 9. Severe injury on the same lower limb affecting functional assessment (such as open fractures, neurovascular injuries).

Design outcomes

Primary

MeasureTime frame
Number of intraoperative fluoroscopies;

Secondary

MeasureTime frame
Surgery duration;Intraoperative blood loss;Fracture healing time;Majeed Pelvic Function Score;Postoperative fracture reduction quality;Intraoperative and postoperative complications;

Countries

China

Contacts

Public ContactChen Hua

The Fourth Medical Center of the Chinese People's Liberation Army General Hospital

chenhua0270@126.com+86 139 1006 8413

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026