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optimization of perioperative protocol according to enhanced recovery after surgery: a prospective randomized controlled study of reducing the predefined tourniquet pressure for traumatic patients

optimization of perioperative protocol according to enhanced recovery after surgery: a prospective randomized controlled study of reducing the predefined tourniquet pressure for traumatic patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059867
Enrollment
Unknown
Registered
2022-05-13
Start date
2022-06-01
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

Extremity fresh fracture

Interventions

Upper extremity treatment Group:Define the tourniquet pressure based on systolic pressure
Upper extremity control group:Tourniquet pressure 250mmHg
Lower extremity treatment group:Define the tourniquet pressure based on systolic pressure
Lower extremity control group:Tourniquet pressure 300mmHg

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age range from 16 to 70 years old, no gender limitation; 2. Upper or lower extremity fresh fracture (less than 3 weeks) and tourniquet needed; 3. Patients who volunteered to participate in this study, and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with peripheral vascular disease, such as varicosity and angiitis obliterans; 2. Patients with deep vein thrombosis preoperatively; 3. Patients with homeopathic disease, such as sickle cell anemia; 4. Patients with preoperative usage of anticoagulant or antiplatelet drugs; 5. Open fracture patients; 6. Systolic pressure more than 200mmHg and not responding to drugs; 7. Other patients who were considered unsuitable for this study by researchers.

Design outcomes

Primary

MeasureTime frame
Grading score of hemostatic effect by surgeon;

Secondary

MeasureTime frame
Postoperative complications;Extremity circumference;Complication rate;

Countries

China

Contacts

Public ContactZhijian Sun

Beijing Jishuitan Hospital

sunzhijian258@163.com+86 13466560932

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026