Actively Recruiting
Tegileridine Combined With Intercostal Nerve Block After Thoracoscopic Lung Resection
Led by Tongji Hospital · Updated on 2026-04-08
118
Participants Needed
1
Research Sites
45 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Combining tegileridine PCIA with ICNB targeting peripheral nerves, may constitute an ideal analgesic model with complementary advantages. Thus potentially achieving the analgesic goal of "early pain relief, stable throughout the process, and rapid recovery," and may have a positive impact on reducing CPSP.
CONDITIONS
Official Title
Tegileridine Combined With Intercostal Nerve Block After Thoracoscopic Lung Resection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 75 years
- Undergoing elective thoracoscopic lobectomy or segmentectomy
- ASA classification I to III
- Body mass index (BMI) between 18 and 30 kg/m2
- Voluntary participation with signed informed consent
You will not qualify if you...
- Preoperative alcohol dependence or long-term use of analgesic drugs for other pain
- Pregnant or lactating women
- Allergies or contraindications to anesthetics, analgesics, or antiemetic drugs used in this study
- Severe sleep apnea syndrome or acute/severe bronchial asthma
- Mental or neurological disorders, cognitive impairment, gastrointestinal obstruction
- Severe liver or kidney dysfunction (Child Pugh score C)
- Chronic obstructive pulmonary disease or severe cardiovascular disease
- Any condition deemed unsuitable by researchers or refusal to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tongji hospital
Wuhan, Hubei, China, 430030
Actively Recruiting
Research Team
A
Aijun Xu, Dr.
CONTACT
H
Hongbo Zheng, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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