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Effects of combined pericapsular nerve group block with transcutanclus electrical acupoint stimulation on total hip arthroplasty

Effects of combined pericapsular nerve group block with transcutanclus electrical acupoint stimulation on total hip arthroplasty

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005873
Enrollment
Unknown
Registered
2022-04-16
Start date
2022-04-11
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Posterolateral approach total hip arthroplasty

Interventions

Group TEAS:Before spinal anesthesia, bilateral Hegu, Neiguan and Zusanli will be subjected to percutaneous acupoint electrical stimulation for 30 minutes.
Group PENG+TEAS:Before spinal anesthesia, bilateral Hegu, Neiguan and Zusanli will be subjected to percutaneous acupoint electrical stimulation for 30 minutes. And ultrasound-guided PENG block will be
Group PENG:Ultrasound-guided PENG block will be performed on the operative hip joint, and 0.5% Ropivacaine injection 20mL will be injected.

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients will be included if they: (1) have an American Society of Anesthesiologists physical status (ASA) between I-?;(2)are at the age of 40 to 65 years old and (3) have a body mass index (BMI) between 18-30kg/m2.

Exclusion criteria

Exclusion criteria: Patients will be excluded if they: (1) refuse to participate in the study; (2) have an allergy to the drug in this study; (3) have a disease of peripheral nerve; (4) have an infection near the block site; (5) have clinically significant neurological, cardiovascular, renal, or hepatic disease (ASA ?-?); (6) have dementia; (7) are pregnant and lactating women; or (8) have a cerebral infarction, lumbar disc herniation and other effects resulting in sensory and motor abnormalities;(9) are suffering severe pain that need the opioids therapy or (10) BMI 30 kg/m2.

Design outcomes

Primary

MeasureTime frame
hospital stay after surgery;QoR-15;

Secondary

MeasureTime frame
the first time of postoperative out-of-bed mobilization;The time of the bolus;the visual analogue scale on movement;Rescue analgesic use;the visual analogue scale at rest;the strength of the quadriceps;the morphine consumption;Postoperative complications;

Countries

China

Contacts

Public ContactWei Luo
yu9luowei0@163.com+8615915860995

Outcome results

None listed

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