Tongji hospital
Wuhan, Hubei, 430030, China
Location status: Recruiting
Location contact
Aijun Xu, Dr.
CONTACT
aihua Du, Dr.
CONTACT
NCT Number: NCT07386626
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.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Not applicable
Wuhan, Hubei, 430030, China
Location status: Recruiting
Aijun Xu, Dr.
CONTACT
aihua Du, Dr.
CONTACT
Combining tegileridine PCIA with ICNB targeting peripheral nerves, may constitute an ideal analgesic model with complementary advantages. ICNB provides rapid and precise incision analgesia in the early postoperative period, effectively blocking the transmission of peripheral nociceptive stimuli to the central nervous system. tegileridine PCIA, on the other hand, enhances the function of the endogenous descending pain suppression system through its central G protein pathway activation, covering the pain period after the effect of ICNB wears off and components such as visceral referred pain. At the same time, it can effectively reduce side effects such as respiratory depression and nausea/vomiting, 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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administer 0.015 mg/kg (maximum 1mg) of tegileridine intravenously 40 minutes before the end of surgery, followed by the connection of a tegileridine patient-controlled intravenous analgesia (PCIA)
Other names: Tegi
Before closing the chest, the thoracic surgeon injected 3mL of 0.4% ropivacaine into the 4th, 5th, 6th and 7th intercostal spaces through thoracoscopy for intercostal nerve block.
Other names: ICNB
Administer 0.15 μg/kg (maximum 10 μg) of sufentanil intravenously 40 minutes before the end of surgery, followed by the connection of a sufentanil patient-controlled intravenous analgesia (PCIA)
Other names: Sufen
Time frame: 48 hours
VAS pain score 0-10, the higher scores mean a worse outcome; Analgesic effect assessed during activity in the post-anesthesia care unit (PACU) and at 1, 6, 12, 24, 36, and 48 hours post-surgery
Time frame: 48hours
The total consumption of remedial analgesic drugs within 48 hours post-surgery
Time frame: 48 hours
Including total analgesic consumption, number of effective presses, and total number of presses
Time frame: 48 hours
Including Respiratory depression (defined as respiratory rate < 8 breaths/min or SpO₂ < 90%); ② Postoperative nausea and vomiting (PONV); ③ Pruritus; ④ Dizziness; ⑤ Delayed recovery of gastrointestinal function, etc.
Time frame: 10 days
The length of postoperative hospital stay from the end of surgery to hospital discharge
Time frame: 10 days
AIS sleep scale was used to assess the quality of sleep
Time frame: 48 hours
the number of rescue analgesic interventions within 48 hours post-surgery
Time frame: 10 days
overall patient satisfaction post-surgery
Contact information is provided by the study sponsor or research team.
Aijun Xu, Dr.
CONTACT
Hongbo Zheng, Dr.
CONTACT
Tongji Hospital
Other
Study on the Analgesic Effect of Tegileridine Combined With Intercostal Nerve Block After Thoracoscopic Lung Resection
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07660900
Force Measurement, Lobectomy
Columbus, Ohio, United States
View Trial DetailsNCT07626489
Infiltration Anesthesia, Lobectomy
Beijing, Beijing Municipality, China
View Trial DetailsNCT07646288
Bronchial Neoplasms, Carcinoma, Bronchogenic
Ankara, Altındağ, Turkey (Türkiye)
View Trial DetailsNCT07055191
Lobectomy, Thyroidectomy
Bobigny, France
View Trial Details