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Recruiting NCT07745881

NCT07745881 Analgesic Effects of Retro-superior Costotransverse Ligament Space Block for Video-assisted Thoracoscopic Surgery

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Clinical Trial Summary
NCT ID NCT07745881
Status Recruiting
Phase —
Sponsor Nanjing First Hospital, Nanjing Medical University
Condition Nerve Block
Study Type INTERVENTIONAL
Enrollment 130 participants
Start Date 2026-08-05
Primary Completion 2028-05-20

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Ultrasound-guided retro-SCTLBUltrasound-guided TPVB

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 130 participants in total. It began in 2026-08-05 with a primary completion date of 2028-05-20.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim of this clinical trial is to investigate the effects of postoperative analgesia during retro-SCTLB(retro superior costotransverse ligament space block) and TPVB(thoracic paravertebral block) in patients undergoing thoracoscopic radical resection of lung cancer。By comparing the dosage of opioid drugs after surgery, the impact of retro-SCTLB and TPVB on the postoperative analgesic effect was evaluated.

Eligibility Criteria

Inclusion Criteria: * Patients scheduled for thoracoscopic radical lung cancer surgery under general anesthesia; * aged 18-80 years; * BMI 18-30 kg/m²; * ASA classification I-III; Exclusion Criteria: * 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; * Dysfunction of blood coagulation;

Contact & Investigator

Central Contact

Tao Shan

✉ shantao2021@163.com

📞 18852095135

Frequently Asked Questions

Who can join the NCT07745881 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Nerve Block. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07745881 currently recruiting?

Yes, NCT07745881 is actively recruiting participants. Contact the research team at shantao2021@163.com for enrollment information.

Where is the NCT07745881 trial being conducted?

This trial is being conducted at Nanjing, China.

Who is sponsoring the NCT07745881 clinical trial?

NCT07745881 is sponsored by Nanjing First Hospital, Nanjing Medical University. The trial plans to enroll 130 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology