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The Relationship Between NLR and PONV and ESPB

Q

Qianfoshan Hospital

Status and phase

Not yet enrolling
Phase 1

Conditions

Erector Spinae Plane Block
Neutrophil to Lymphocyte Ratio

Treatments

Procedure: 0.9% physiological saline (20ml) injection under ultrasound-guided Erector Spinae Plane Block (ESPB).
Procedure: Erector Spinae Plane Block

Study type

Interventional

Funder types

Other

Identifiers

NCT06127966
YXLL-KY-2023(101)

Details and patient eligibility

About

This study aims to investigate whether preoperative NLR (Neutrophil-to-Lymphocyte Ratio) serves as a biomarker for PONV (Postoperative Nausea and Vomiting). It also examines the impact of erector spinae plane block on NLR and PONV. Furthermore, the research explores the effect of erector spinae plane block on postoperative pain relief in spinal surgery and its influence on the usage of opioid medications.

Enrollment

220 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients undergoing elective posterior lumbar spine surgery in a prone position under general anesthesia.
  2. ASA classification grades I to II.
  3. Age between 18 and 80 years old.
  4. Signed the informed consent for this study.

Exclusion criteria

  1. Preoperative blood transfusion.
  2. Uncontrolled systemic diseases.
  3. Gastrointestinal system disorders.
  4. History of antiemetic and anticholinergic drug use.
  5. Adverse reactions related to surgery.
  6. Severe spinal deformities.
  7. Infection at the puncture site.
  8. Coagulation disorders.
  9. Long-term use of sedatives and analgesic drugs before surgery.
  10. Patients with mental illness or communication barriers.
  11. Allergic to ropivacaine.
  12. Participants involved in other clinical studies within the past 3 months.
  13. History of previous lumbar surgeries.
  14. Subjective unwillingness to participate in this study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

220 participants in 2 patient groups

Erector Spinae Plane Block group(EA group + EB group)
Experimental group
Description:
Conventional anesthesia induction, followed by ultrasound-guided erector spinae plane (ESPB) block with 0.5% ropivacaine (20 ml) after anesthesia induction.
Treatment:
Procedure: Erector Spinae Plane Block
Control group(CA group + CB group)
Sham Comparator group
Description:
Conventional anesthesia induction, followed by ultrasound-guided injection of 0.9% saline (20 ml) into the erector spinae plane (ESPB) after anesthesia induction.
Treatment:
Procedure: 0.9% physiological saline (20ml) injection under ultrasound-guided Erector Spinae Plane Block (ESPB).

Trial contacts and locations

0

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Central trial contact

Guanghan Wu, Attending physician

Data sourced from clinicaltrials.gov

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