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0.15 mg Spinal Morphine vs. no Treatment for Morphine Requirement After VATs.

M

Mahidol University

Status and phase

Unknown
Phase 4

Conditions

Postoperative Pain

Treatments

Drug: Spinal morphine

Study type

Interventional

Funder types

Other

Identifiers

NCT01979354
552/2556(EC3)

Details and patient eligibility

About

Postoperative pain after Video-assisted Thoracoscopic Surgery (VAT) is still debating. Therefore the investigators conduct a study comparing 0.15 mg spinal morphine and control group in term of analgesia.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 year or over
  • Patient ASA physical status I-III.
  • Scheduled for video-assisted thoracoscopic lobectomy or blebectomy with pleurectomy or pleural abrasion
  • Can operate a patient-controlled analgesia (PCA) device.

Exclusion criteria

  • Known hypersensitivity to morphine
  • History of bleeding tendency.
  • Known case of infection at the back
  • Patient refuse for spinal anesthesia
  • History of cerebrovascular disease.
  • Need mechanical ventilatory support during postoperative period

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

40 participants in 2 patient groups

Spinal morphine
Active Comparator group
Description:
0.15 mg spinal morphine
Treatment:
Drug: Spinal morphine
Control
No Intervention group
Description:
No spinal morphine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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