The efficacy and safety of continuous thoracic paravertebral block on postthoractomy pain: a prospective, randomized and single center study

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037360

Enrollment

Unknown

Registered

2020-08-28

Start date

2021-10-30

Completion date

Unknown

Last updated

2020-10-19

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

Conditions

Chronic postthoractomy pain

Interventions

Group A:thoracic epidural analgesia

Group B:continuous thoracic paravertebral block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. adult patients that are planned to have thoractomies in our institution; 2. educated over 9 years; 3. ethical approval and patient consent; 4. associated tests completed, including.

Exclusion criteria

Exclusion criteria: 1. cognitive dysfunction/difficulty in communication; 2. severe cardivascular/cerebral dysfunction, hepatic or renal dysfunction; 3. coagulation dysfunction or digestion of anti-coagulants in the past week; 4. spinal deformity or spinal sugery history; 5. preoperative analgesics ingestion or othe drug dependence; 6. pain in the back or infection/lump in the puncture boundary.

Design outcomes

Primary

Measure	Time frame
CPTP incidence after 3 months;CPTP incidence after 6 months;	—

Secondary

Measure	Time frame
posthoractomy pain incidence in 24hours;posthoractomy pain incidence in 48hours;	—

Countries

China

Contacts

Public ContactGu Yang

Shanghai Pulmonary Hospital

896274362@qq.com+86 15921552347

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026