Skip to content

Efficacy of Graded Intermittent Pneumatic Compression Therapy in Preventing Deep Vein Thrombosis Following Spinal Surgery

Efficacy of Graded Intermittent Pneumatic Compression Therapy in Preventing Deep Vein Thrombosis Following Spinal Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125529
Enrollment
Unknown
Registered
2026-05-28
Start date
2026-06-05
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Spinal degenerative diseases

Interventions

Experimental group:For Caprini score moderate risk: IPC treatment twice daily, 1 hour per session. For Caprini score high risk: IPC treatment three times daily, 1 hour per session. For Caprini score v
Control group:For all patients with moderate, high, or very high Caprini risk: IPC twice daily, 30 minutes per session.

Sponsors

The Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 80 years, with complete clinical data; 2.Diagnosed with spinal disease and scheduled to undergo elective or emergency spinal surgery; 3.The Caprini thrombosis risk assessment score indicates a moderate-risk or higher level of risk; 4.Conscious, without severe cognitive or communication impairment, able to understand and cooperate with the study interventions and assessments; 5.Willing to participate voluntarily in this study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with lower extremity deep vein thrombosis (DVT) or pulmonary embolism (PE) by imaging examination upon admission; 2.Presence of active bleeding or high risk of bleeding (e.g., known severe coagulation disorders, active peptic ulcer, history of intracranial hemorrhage, etc.); 3.Severe peripheral arterial disease, or conditions of the lower limbs unsuitable for the use of intermittent pneumatic compression devices (e.g., dermatitis, infection, severe edema, open wounds, etc.); 4. Combined severe cardiac, hepatic, or renal insufficiency (as determined by the attending physician's clinical diagnosis); 5. Women who are pregnant or breastfeeding; 6. Concurrent participation in other clinical trials that may interfere with the outcomes of this study.

Design outcomes

Primary

MeasureTime frame
The peak flow velocities of blood flow in the common femoral vein and the popliteal vein;

Secondary

MeasureTime frame
The incidence rate of VTE;D-dimer concentration;Fibrinogen concentration;Platelet count;

Countries

China

Contacts

Public ContactLuo Chunmei

The Second Affiliated Hospital of the Army Medical University

812886960@qq.com+86 177 8475 8331

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026