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programmed intermittent bolus infusion for postoperative analgesia with fascia iliaca compartment block catheter after arthroscopic cruciate ligament surgery

programmed intermittent bolus infusion for postoperative analgesia with fascia iliaca compartment block catheter after arthroscopic cruciate ligament surgery: a randomized, double-blind, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091003
Enrollment
Unknown
Registered
2024-10-17
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

cruciate ligament surgery

Interventions

PIB Group:Patients in programmed intermittent pulse infusion group (PIB group) received ultrasound-guided fascia iliaca compartment block catheterization after tracheal intubation of general anaesth
CI Group:Patients in continue infusion group (CI group) received ultrasound-guided fascia iliaca compartment block catheterization after tracheal intubation of general anaesthesia. patient-control a

Sponsors

Shantou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. patients who underwent knee arthroscopic cruciate ligament reconstruction under general anaesthesia with endotracheal intubation; 2. aged 18-64 years; 3. postoperative analgesia by fascia iliaca compartment block catheter; 4. complete clinical history, signs, and examinations; 5. understanding, voluntary participation in the study, signing of the informed consent form, and the ability to communicate fluently.

Exclusion criteria

Exclusion criteria: 1. patients who underwent bilateral knee arthroscopy or other surgical treatments at the same time; 2. patients who were allergy to the drugs related to this study; 3. suffering from severe diabetes mellitus; 4. having neuromuscular disorders in the affected limbs with abnormal muscle strength or sensation before the operation, which affects the clinical assessment; 5. special population groups such as pregnant women.

Design outcomes

Primary

MeasureTime frame
postoperative pain scoring at rest and on movement;

Secondary

MeasureTime frame
Nerve block status (lateral femoral cutaneous nerve, femoral nerve, obturator nerve);Walking on crutches;Flexibility angle of joints;Anesthesia and surgery factors;Dose of anesthetics;fluid Infusion dose;

Countries

China

Contacts

Public ContactWenjun Ma

Shantou central hospital

499262579@qq.com+86 136 7035 8377

Outcome results

None listed

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