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NCT07153263Recruiting

Local Anaesthetic Spread and Sensory Block Range of the Retro-superior Costotransverse Ligament Space Block

Comparison of Local Anaesthetic Spread Between the Retro-superior Costotransverse Ligament Space Block and Thoracic Paravertebral Block: A Three-dimensional CT Reconstruction Imaging Study

Source: ClinicalTrials.gov · Last updated 28 Aug 2026

Brief summary (registry, in English)

The aim of this clinical trial is to investigate the effects of local anesthetic diffusion range and sensory block range during retro-SCTLB(retro superior costotransverse ligament space block) and TPVB(thoracic paravertebral block) in patients undergoing CT-guided lung nodule localization. The main issue of the study is to determine the differences in the diffusion range and sensory block range of local anesthetics between the retro-SCTLB and TPVB nerve block methods.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
21 Aug 2025
Start date
12 Sept 2025
Primary completion date
15 Sept 2026
Lead sponsor
Nanjing First Hospital, Nanjing Medical University
NCT number
NCT07153263

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 12 Sept 2025 to the primary completion date, 15 Sept 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Allergy to the study drug or local anesthetic;
  • History of opioid abuse;
  • Pre-existing skin infection at the puncture site of ITPN or TPVB;

Other

  • Peripheral infectious neuropathy;
  • Dysfunction of blood coagulation

Who the study is looking for

  • Patients scheduled for CT-guided lung nodule localization under local anesthesia will be selected
  • aged 18-80 years
  • BMI 18-30 kg/m²
  • ASA classification I-III

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nanjing First Hospital
Coordinator of this site? Confirm its status
NanjingChinaRecruiting
Tao Shan
Coordinator of this site? Confirm its status
NanjingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.