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Efficacy of thoracic wall block for breast cancer operation -randomized double blind study-.

Efficacy of thoracic wall block for breast cancer operation -randomized double blind study-. - Efficacy of thoracic wall block for breast cancer operation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013435
Enrollment
120
Registered
2014-03-17
Start date
2014-03-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast cancer

Interventions

Thoracic wall block with 0.25% levobupivacaine was performed in the anesthesia for Thoracic wall block with 0.25% levobupivacaine was performed in the anesthesia for breast cancer sugery As control, t

Sponsors

Niigata University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: The female patients who will undergo breast cancer surgery in Niigata University Hospital (from 20 y.o to 80 y.o.)

Exclusion criteria

Exclusion criteria: The patient who disagree to participate in this study ASA-physical status =/>4 The patient who has difficulty for communication (eg. patient suffered from dementia, has mental retardation, can not understand Japanese) Body Mass Index >30kg/m2 Body Weight<40kg The patient has allergy for the drugs that will use in this study Renal dysfunction or hepatic dysfunction The patient who has abnormal sensation or hypoesthesia in body trunk The patient who is received opioid medication The patient whom the examiner assume inadequate to participate in this study

Design outcomes

Primary

MeasureTime frame
intraoperative: dose of anesthetics (propofol) and opioid (remifentanil) postoperative: incidence of usage of adjuvant analgesics and spontaneous pain scale (numerical rating scale)

Secondary

MeasureTime frame
intraoperative: anesthetic induction time postopreative: incidence and degree of postoperative nausea and vomiting, incidence of adverse event and incidence and degree of persistent postoperative pain at 1,3 and 6 month after surgery

Countries

Japan

Contacts

Public ContactHiroshi Baba

Niigata University Graduate School of Medical and Dental Science Anesthesiology

baba@med.niigata-u.ac.jp025-227-2328

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026