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Study on the effect of ischemic preconditioning combined with femoral nerve and femoral artery block on intra-operative tourniquet hypertension in patients undergoing knee joint surgery

Study on the effect of ischemic preconditioning combined with femoral nerve and femoral artery block on intra-operative tourniquet hypertension in patients undergoing knee joint surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098660
Enrollment
Unknown
Registered
2025-03-12
Start date
2024-03-25
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

tourniquet hypertension

Interventions

control group:none
modified femoral nerve block group:modified femoral nerve block performed 40 minutes preoperatively
Ischaemic preconditioning group:Ischaemic preconditioning operation 40 minutes before surgery
modified femoral nerve block block + ischaemic preconditioning (IPC) combined intervention group:modified femoral nerve block and ischemic preconditioning were performed 40 minutes before surgery.

Sponsors

The First People's Hospital of Qujing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients who are going to undergo knee surgery under general anaesthesia in the operating theatre of the First People's Hospital of Qujing and need to use a tourniquet. Knee surgeries include total knee arthroplasty, arthrocleansing, cartilage repair, meniscectomy, meniscus repair, ligament reconstruction, osteotomy, and arthroplasty fusion. (2) Aged 18-75 years old; (3) BMI of 18-28 kg/m^2; (4) Voluntary signed informed consent;

Exclusion criteria

Exclusion criteria: (1) Patients with ASA >= grade IV; (2) Patients with contraindications to the drugs or any of the anaesthetic methods in this study (nerve block puncture site infection, allergy to anaesthetic drugs); (3) Tourniquet inflation time 150 minutes. (4) Patients with long-term anticoagulation; (5) Chronic pain and long-term use of opioid analgesic drugs; (6) Uncontrolled hypertension (systolic blood pressure >=160mmHg or diastolic blood pressure >=110mmHg in sitting position; systolic blood pressure 20mmHg. (8) Contraindications to tourniquet (peripheral vascular disease, peripheral neuropathy, previous arterial bypass graft and popliteal artery calcification); (9) Patients with previous knee surgery on the affected limb. (10)Patients with diabetes mellitus with poor glycaemic control (random blood glucose >=11.1 mmol/L).

Design outcomes

Primary

MeasureTime frame
Intraoperative systolic pressure ;

Secondary

MeasureTime frame
Detection of serum levels of inflammatory factors TNF-a, IL-6;Detection of serum levels of SOD, MDA;Detection of serum levels of iNOs, eNOs;Plasma D-dimer levels;FDP levels in plasma;Plasma levels of vWF;TM levels in plasma;VAS scores of patients;

Countries

China

Contacts

Public ContactJiangang Li

The First People's Hospital of Qujing

77684698@qq.com+86 874 332 1147

Outcome results

None listed

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