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Comparison of the effects of ultrasound-guided regional block with different approaches on postoperative rehabilitation after knee arthroscopy

Comparison of the effects of ultrasound-guided regional block with different approaches on postoperative rehabilitation after knee arthroscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049287
Enrollment
Unknown
Registered
2021-07-29
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

None listed

Interventions

Group AC :through the adductor canal
Group FT:via the femoral triangle

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Approved by the ethics committee and informed consent of the patient. 2. The patient's anesthesia ASA classification is grade I-II, and the aged 18-65 years (including 18 years old and 65 years old). 3. Patients undergoing elective unilateral knee arthroscopy. 4. Volunteer experiment. The process of obtaining informed consent should comply with GCP regulations.

Exclusion criteria

Exclusion criteria: 1. The puncture site has infection and coagulation dysfunction. 2. Patients who are allergic to local anesthetics, allergic constitution. 3. Those with a history of mental or nervous system diseases or combined with traumatic brain injury and unable to communicate normally. 4. Lower extremity neuromuscular disease. 5. Those with a history of epilepsy, alcoholism, or taking illegal drugs. 6. According to the judgment of the investigator, other diseases that reduce the possibility of enrolling or complicate enrollment, such as frequent changes in the working environment, are likely to cause loss to follow-up. 7. Patients who are participating in clinical trials of other drugs.

Design outcomes

Primary

MeasureTime frame
First time out of bed;''Stand up and walk'' timing test time;Quadriceps strength;Knee range of motion;The number of steps on the pedometer at 48 hours postoperatively;

Secondary

MeasureTime frame
VAS scores at rest and during exercise;Dosage of analgesic relief drugs;Postoperative hospital stay;Adverse reactions;The satisfaction of patients;

Countries

China

Contacts

Public ContactHuang Lan

Affiliated Hospital of Nanjing University of Chinese Medicine

1437548193@qq.com+86 19524266309

Outcome results

None listed

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