Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorNanjing First Hospital, Nanjing Medical University
About this trial
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.
Eligibility criteria
Qualifiers
aged 18-80 years
BMI 18-30 kg/m²
ASA classification I-III
Disqualifiers
Allergy to the study drug or local anesthetic;
History of opioid abuse;
Pre-existing skin infection at the puncture site of ITPN or TPVB;
Peripheral infectious neuropathy;
Trial design
Treatments tested in this trial
- Ultrasound-guided retro-SCTLB
- Ultrasound-guided TPVB
Treatment groups
50 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov