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Ultrasound Guided Thoracic Paravertebral Block for Hepatic Tumors Ablation

M

Mahidol University

Status

Completed

Conditions

Liver Cancer

Treatments

Drug: 0.5% marcaine 20ml

Study type

Interventional

Funder types

Other

Identifiers

NCT02271646
070/2557(EC2)
(IO) R015731063 (Other Grant/Funding Number)

Details and patient eligibility

About

Patients undergo percutaneous radiofrequency ablation of hepatic tumors at Siriraj hospital normally receive only intravenous sedative drugs which sometimes can not provide effective pain control.

TPVB is suitable for unilateral operations. And it is increasing popular nowadays because of using ultrasound guided which make it is more reliable and has less side effects especially the severe one such as pneumothorax. To cover all nerve supply liver, we decided to use right TPVB at T5-6, T7-8, and T9-10.

The aim of this study is to prove that TPVB can provide an effective pain control for patients undergo liver RFA both at rest and movement (cough). We are going to measure the pain score at recovery room and the effective pain control means patients has mild pain (pain score less </= 3 and do not ask for analgesic drugs).

Enrollment

35 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years
  • Patients undergo percutaneous radiofrequency ablation for liver tumors
  • ASA classification 1-3

Exclusion criteria

  • Psychiatric illness
  • Chronic abdominal pain > 1 week
  • Regular analgesic drugs use
  • Infection at back (Block area)
  • Severe spinal deformity
  • PT > 16 sec, aPTT > 32, platelet < 50,000/cumm

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

35 participants in 1 patient group

0.5% marcaine 20ml
Experimental group
Description:
3 levels ultrasound guided thoracic paravertebral blocks at T5-6, T7-8 and T9-10 (total 0.5% marcaine 20ml)
Treatment:
Drug: 0.5% marcaine 20ml

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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