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Comparison of Different Neural Blockade Techniques in Postoperative Analgesia After Total Hip Arthroplasty

T

Taichung Veterans General Hospital

Status

Unknown

Conditions

Pain, Postoperative

Treatments

Procedure: Fascia iliaca compartment block with IV-PCA
Procedure: IV-PCA
Procedure: Femoral nerve block and lateral femoral cutaneous nerve with IV-PCA

Study type

Interventional

Funder types

Other

Identifiers

NCT03231319
CF17089A

Details and patient eligibility

About

To compare the different analgesic protocols for patients receiving total hip arthroplasty(THA). Patients will divided into 3 groups, which are 1. fascia iliaca compartment block with IV-PCA(patient controlled analgesia), 2. femoral nerve and lateral femoral cutaneous nerve block with IV-PCA, 3. IV-PCA only.

Full description

90 patients will be enrolled and randomized to the 3 different groups.

  1. Inclusion criteria:

    Patient undergoing THA: 20-75 years old, ASA I-III, general anesthesia with intubation, fentanyl IV PCA.

  2. Exclusion criteria Alcohol/substance abuse Rheumatoid arthritis Severe coagulation disorder(PLT<80000 or INR > 1.5) Peripheral neuropathy Allergy to opioids or local anesthetics BMI>35

  3. The outcome followers are blinded to the intervention provided.

  4. Outcome parameters:

    1. Opioid consumption of IV PCA in first 24 hrs.

    2. NSAID consumption

    3. NRS of pain, the timings of follow-up should be: pre-block, 30

      mins post-block, 60 mins post-block, 2 hours post-block, 24hours post-block

    4. sensory block in FN, Obturator Nerve and LFCN

    5. First request of supplemental IV analgesia

Enrollment

90 estimated patients

Sex

All

Ages

20 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-III, general anesthesia with intubation.
  • fentanyl IV PCA

Exclusion criteria

  • Alcohol/substance abuse
  • Rheumatoid arthritis
  • Severe coagulation disorder(PLT<80000 or INR > 1.5)
  • Peripheral neuropathy
  • Allergy to opioids or local anesthetics
  • BMI>35

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups, including a placebo group

fascia iliaca compartment block+ IV-PCA
Active Comparator group
Treatment:
Procedure: Fascia iliaca compartment block with IV-PCA
femoral nerve and lateral femoral cutaneous nerve block+IV PCA
Active Comparator group
Treatment:
Procedure: Femoral nerve block and lateral femoral cutaneous nerve with IV-PCA
IV PCA only
Placebo Comparator group
Treatment:
Procedure: IV-PCA

Trial contacts and locations

2

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Central trial contact

Chih-Cheng Wu, M.D.; Tsung-Yung Tang, M.D.

Data sourced from clinicaltrials.gov

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