Comparison of ultrasound-guided high ankle block and lumbar anaesthesia for rapid recovery from day surgery of the foot and ankle

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300077254

Enrollment

Unknown

Registered

2023-11-02

Start date

2023-11-02

Completion date

Unknown

Last updated

2023-11-06

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

Conditions

Acute postoperative pain

Interventions

Group N:Ultrasound-guided high ankle nerve block

Group S :Subarachnoid block

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Agreed to participate in this study and signed the informed consent form; 2. Patients aged =18 years with junior high school education and above; 3. American Society of Anaesthesiologists (ASA) grade I-III; 4. Patients who underwent day surgery of the foot and ankle (unilateral synovectomy of the foot and ankle, free body removal, joint adhesion release, articular osteochondral repair, simple fracture reduction and internal fixation, ankle clean-up or ligament repair and reconstruction, and other non-serious injuries or disease surgery).

Exclusion criteria

Exclusion criteria: 1. BMI =40kg/m2; 2. Those with a history of allergy to local anaesthetics, contraindication to intrathecal anaesthesia and nerve block anaesthesia; 3. Those who suffer from serious heart, liver, lung, kidney and other vital organ diseases; 4. Those suffering from serious infectious diseases, peripheral nerve diseases, immune system diseases and blood system diseases; 5. cognitive or mental dysfunction resulting in the inability to communicate verbally for pain scoring; 6. Those who are pregnant; 7. Those who have recently received chronic pain treatment.

Design outcomes

Primary

Measure	Time frame
QoR-15 scale score;	—

Secondary

Measure	Time frame
Sensory scores, motor scores and the effect of anaesthesia;Pain numericalratingscale;Sensory complete block time, motor complete block time, postoperative sensory recovery time, motor recovery time;Dosage of anaesthetic drugs, time to first postoperative remedial analgesia, number of remedial analgesia and dosage of analgesic drugs within 48h, remedial analgesia rate;Changes in blood levels of IL-6, IL-1ß, and TNF-a in the median elbow vein;	—

Measure

Time frame

Sensory scores, motor scores and the effect of anaesthesia;Pain numericalratingscale;Sensory complete block time, motor complete block time, postoperative sensory recovery time, motor recovery time;Dosage of anaesthetic drugs, time to first postoperative remedial analgesia, number of remedial analgesia and dosage of analgesic drugs within 48h, remedial analgesia rate;Changes in blood levels of IL-6, IL-1ß, and TNF-a in the median elbow vein;

—

Countries

China

Contacts

Public ContactWang Kai

Xuzhou Central Hospital

wangkaistream99@sina.com+86 181 1201 2729

Outcome results

None listed

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