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Effect of catheter tip location on the spread of sensory block produced by continuous thoracic paravertebral block: a prospective, randomized, double-blind study

Effect of catheter tip location on the spread of sensory block produced by continuous thoracic paravertebral block: a prospective, randomized, double-blind study - Effect of catheter tip location on the spread of sensory block produced by continuous thoracic paravertebral block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000018578
Enrollment
50
Registered
2015-08-07
Start date
2015-08-07
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

Patients scheduled for a unilateral video-assisted thoracic surgery

Interventions

Catheters will be inserted into the thoracic paravertebral space, where is ventral to the endothoracic fascia, under ultrasound guidance. Catheters will be inserted into the thoracic paravertebral spa

Sponsors

Niigata University Medical and Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients undergoing video-assisted thoracic surgery at Niigata University Medical and Dental Hospital 2. Written informed consent is provided

Exclusion criteria

Exclusion criteria: 1. American Society of Anesthesiologists Physical Status over 4 2. Inability to communicate lucidly 3. Under 20 or over 80 years old 4. Body Mass Index >30 kg/m^2 5. Body weight <40 kg 6. Contraindication or allergy to drugs used in this study 7. Renal or hepatic failure 8. Pre-existing sensory disturbance of the trunk 9. Patients requiring a posterolateral thoracotomy extending within 2 cm from the catheter insertion site 10. Previous ipsilateral thoracotomy 11. Infection at the catheter insertion site 12. Intrathoracic placement of the catheter 13. Patients who are regarded ineligible by researchers with any other reasons

Design outcomes

Primary

MeasureTime frame
Number of anesthetized dermatomes 24 h after surgery

Secondary

MeasureTime frame
Number of anesthetized dermatomes 2 h after surgery Spread of contrast dye injected into the paravertebral space Pain scale Sedation level Incidence of postoperative nausea and vomiting Incidence of local anesthetic systemic toxicity

Countries

Japan

Contacts

Public ContactTakayuki Yoshida

Niigata University Graduate School of Medical and Dental Sciences Division of Anesthesiology

ytaka@mac.com025-227-2328

Outcome results

None listed

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