The effect of intermittent pneumatic compression device in neurosurgery on postoperative lower extremity venous thrombosis

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100053239

Enrollment

Unknown

Registered

2021-11-17

Start date

2021-12-01

Completion date

Unknown

Last updated

2023-05-29

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

Conditions

Craniotomy patient

Interventions

experimental group:IPC device is used intraoperatively

control group:IPC device is not used intraoperatively

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with elective neurosurgical craniotomy; 2. Aged > 18 years; 3. ASA classification I-II.

Exclusion criteria

Exclusion criteria: 1. Coagulopathy defects (activated partial thrombin time 32.5s, Plasma prothrombin time 14s, Thrombin time 21s, Fibrin degradation products < 5mg/L or Plasma D-dimer < 0.55ug/ml ). 2. The patient who is using anticoagulant drugs. 3. Patients who have vascular related diseases within 1 year (arteriovenous thrombosis, post-varicose thrombosis syndrome, peripheral arterial occlusive disease). 4. Pregnant and lactating women. 5. Patient who was participating in other clinical trials

Design outcomes

Primary

Measure	Time frame
Incidence of venous thrombosis;	—

Countries

China

Contacts

Public ContactSun Yongxing

Sanbo Brain Hospital, Capital Medical University

8793705@163.com+86 135 2169 7866

Outcome results

None listed

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