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Clinical Study of Ultrasound-Guided Cutaneous Nerve Block for Lower Limbs in Endovenous Radiofrequency Ablation of the Great Saphenous Vein

Clinical Study of Ultrasound-Guided Cutaneous Nerve Block for Lower Limbs in Endovenous Radiofrequency Ablation of the Great Saphenous Vein

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114259
Enrollment
Unknown
Registered
2025-12-09
Start date
2025-06-24
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

The Pain during endovenous radiofrequency ablation for great saphenous vein varicosities

Interventions

Control group:the tumescent anesthesia
Experimental group:the lower limb cutaneous nerve block

Sponsors

The Fifth Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign the informed consent form; 2. Aged over 20 and under 60, with no gender restrictions; 3. Diagnosed with lower limb varicose veins; 4. Planned to undergo endovenous radiofrequency ablation of the lower limbs; 5. Agree to undergo lower limb superficial nerve block anesthesia.

Exclusion criteria

Exclusion criteria: 1. Presence of contraindications to lower limb cutaneous nerve block anesthesia; 2. Allergy to local anesthetics; 3. Suffering from uncontrolled hypertension, heart failure, myocardial infarction, malignant arrhythmia, or other cardiovascular diseases, or currently experiencing respiratory diseases such as pneumonia, asthma, and obstructive emphysema; 4. Pre-anesthesia risk assessment of ASA grade 4 or above, such as malignant tumors with poor general condition or distant metastasis, severe liver or kidney dysfunction, etc.; 5. Mental disorders making cooperation with anesthesia and the study impossible; 6. Recent or long-term use of analgesic drugs; 7. History of drug abuse; 8. Other conditions deemed by the investigator to be unsuitable for participation in clinical research.

Design outcomes

Primary

MeasureTime frame
the numerical rating scale score;

Secondary

MeasureTime frame
Muscle strength grading of lower limbs;satisfaction of patient and surgeon;the timed up-and-go trial;Anesthesia-related adverse reactions;First postoperative mobilization time;Rescue analgesic dosage;Heart rate;Mean arterial pressure;

Countries

China

Contacts

Public ContactYang Lukun

The Fifth Affiliated Hospital of Sun Yat-sen University

yanglk@mail.sys.edu.cn+86 756 2528355

Outcome results

None listed

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