Skip to content

Comparison of the effects of different anesthesia methods on the surgical duration of lower limb revascularization patients: a retrospective study

Comparison of the effects of different anesthesia methods on the surgical duration of lower limb revascularization patients: a retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100198
Enrollment
Unknown
Registered
2025-04-03
Start date
2025-05-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Lower limb arteriosclerosis obliterans

Interventions

Neuroblock group:None
Anesthesia Monitoring Group:None

Sponsors

Zhongshan Hospital, Fudan University(Xiamen Branch)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Lower limb ASO patients underwent intracavitary intervention treatment at Xiamen Hospital affiliated with Fudan University. 2. Surgical time >= 60 minutes. 3.Age greater than or equal to 45 years old. 4.The anesthesia method is nerve block (iliac fascia combined with sciatic nerve block) or MAC. 5. The patient is informed and agrees, and signs an informed consent form. 6. At least one of the following risk factors is still present 1. Age >=60 years old 2. The patient experienced clinical symptoms such as intermittent claudication, resting pain, and lower limb ulcers before surgery 3. Merge hypertension requiring medication treatment 4. Combination of diabetes requiring drug or insulin treatment 5. Coronary atherosclerotic heart disease 6. Smoking history and failure to quit smoking 7. Preoperative blood creatinine >=175umol/l

Exclusion criteria

Exclusion criteria: 1.Severe coagulation dysfunction accompanied by spontaneous bleeding or anesthesia. The attending physician determines that the bleeding tendency is severe and not suitable for regional blockade 2. Acute exacerbation of preoperative heart failure 3. The patient is at risk of infection 4. The patient refused to participate in the study.

Design outcomes

Primary

MeasureTime frame
Surgical duration;The incidence of intraoperative adverse reactions;

Secondary

MeasureTime frame
Postoperative complications;

Countries

China

Contacts

Public ContactMeijing Ying

Zhongshan Hospital, Fudan University(Xiamen Branch)

ying.meijing@zsxmhospital.com+86 157 1068 8406

Outcome results

None listed

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