Perioperative application of intermittent pneumatic compression in preventing post-laproscopic rectum resection surgery embolism: a randomized controlled trial

Perioperative application of intermittent pneumatic compression in preventing post-laproscopic surgery embolism: a randomized controlled trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000035325

Enrollment

Unknown

Registered

2020-08-08

Start date

2020-08-08

Completion date

Unknown

Last updated

2022-01-24

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

Conditions

rectum cancer

Interventions

IPC feet:IPC is applied in the bilateral feet

IPC crus:IPC is appiled in the bilateral cruses

IPC crus+thigh:IPC is appiled in the bilateral cruses and thighs

controlled group:no IPC application

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Aged > 18 years; 2. Operation interval: 2-4 hour; 3. Normal coagulatory function; 4. No thrombosis; 5. Eager to be involved in the trial.

Exclusion criteria

Exclusion criteria: 1. History of venous thrombosis, phlebitis, severe limb infection; 2. Less of 1 month after cession of anticoagulant; 3. Concumitant of respiratory, circulatory, digestive, neural disorder, incapility of contraction; 4. Ulcerative rash; 5. Abnormal deformity and edema in lower limbs.

Design outcomes

Primary

Measure	Time frame
incidence of embolism;	—

Secondary

Measure	Time frame
flow rate of veins in lower limbs measured by ultrasound;perioperative vWF factors;perioperative coagulatory functions;Lower extremity venous flow under ultrasound;	—

Countries

China

Contacts

Public ContactJiehao Sun

The First Affiliated Hospital, Wenzhou Medical University

sun_jiehao@126.com+86 13676721930

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026