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Oxycodone in Combination With Parathoracic Nerve Block is Used for Postoperative Analgesia in Lung Cancer

Q

Qianfoshan Hospital

Status and phase

Not yet enrolling
Phase 1

Conditions

Oxycodone

Treatments

Drug: Oxycodone 1mg/kg
Drug: Oxycodone 1.5mg/kg
Drug: Sufentanil

Study type

Interventional

Funder types

Other

Identifiers

NCT05742256
YXLL-KY-2022(116)

Details and patient eligibility

About

In this study, the effect of oxycodone combined with ultrasound-guided paravertebral nerve block on the postoperative analgesic effect of thoracoscopic lung cancer was investigated, and the effect and reasonable dose of oxycodone were explored, which provided a reference for the clinical multimodal analgesia after thoracoscopic lung cancer surgery.

Enrollment

159 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male or female, age > 60 years
  2. Patients undergoing thoracoscopic lobectomy
  3. ASA (American Academy of Anesthesiologists) Grades I-III
  4. There were no obvious abnormalities in heart, liver, and kidney function
  5. Sign the informed consent form for this clinical study

Exclusion criteria

  1. History of oxycodone or sufentanil allergy
  2. Renal or hepatic dysfunction
  3. History of drug or alcohol abuse
  4. Psychiatric disorders: schizophrenia, epilepsy, Parkinson's disease, myasthenia gravis
  5. Those who have difficulty communicating due to coma, severe dementia, speech barrier, or those who cannot cooperate due to other diseases.
  6. People with head trauma or other brain diseases -

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

159 participants in 3 patient groups

Test group 1(OCA group)
Experimental group
Treatment:
Drug: Oxycodone 1mg/kg
Test group 2(OCB group)
Experimental group
Treatment:
Drug: Oxycodone 1.5mg/kg
Control group(SF group)
Active Comparator group
Treatment:
Drug: Sufentanil

Trial contacts and locations

0

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Central trial contact

Pengcai Shi, Chief physician

Data sourced from clinicaltrials.gov

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