Xijing Hospital
Xi'an, Shaanxi, 710032, China
Location status: Recruiting
Location contact
Chong Lei, PH.D., M.D.
CONTACT
Lini Wang, M.D.
CONTACT
NCT Number: NCT07271615
The primary objective of this study is to determine the feasibility of preoperative stellate ganglion block in reducing the incidence of postoperative atrial fibrillation in patients undergoing CABG.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Xi'an, Shaanxi, 710032, China
Location status: Recruiting
Chong Lei, PH.D., M.D.
CONTACT
Lini Wang, M.D.
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ultrasound-guided stellate ganglion block with ropivacaine
Time frame: within 7 days postoperatively
Time frame: within 7 days postoperatively
Time frame: within 7 days postoperatively
Time frame: within 7 days postoperatively
Time frame: within 7 days postoperatively
Time frame: duration of postoperative hospital stay
Time frame: within 7 days postoperatively
Contact information is provided by the study sponsor or research team.
Xijing Hospital
Other
Preoperative Stellate Ganglion Block Reduce the Incidence of Postoperative Atrial Fibrillation After Coronary Artery Bypass Grafting: A Prospective, Randomized Controlled Pilot Trial
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.