A Prospective Research on the Differences between Flexiable and Normal Vertebroplasty Tools on Percutaneous Kyphoplasty

Status

Recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1800016453

Enrollment

Unknown

Registered

2018-06-02

Start date

2018-06-01

Completion date

Unknown

Last updated

2018-06-05

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

Conditions

compression fracture of vertabral body

Interventions

control group:aplly normal vertebroplasty tool

experimental group:aplly flexiable vertebroplasty tool

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients complain on pain in the back waist, located the same as the MRI report; 2. The compression of vertebrol body is no more than 2/3 of the normal,and the posterior wall of vertebrol body is complete; 3. VAS pain score of the patients are above 6,

Exclusion criteria

Exclusion criteria: 1. Patients who can not tolerant the surgical procedure; 2. Patients who have coagulation disorders; 3. Patients who are allergic to bone cement; 4. Patients who have active infection.

Design outcomes

Primary

Measure	Time frame
VAS pain socre;ODI socre;leakage of bone cement;operation time;	—

Countries

China

Contacts

Public ContactQingjun Su

Beijing Chaoyang Hosipital

qjsurex@sohu.com+86 13911923253

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026