Ignite Creation Date:
2024-05-06 @ 8:23 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06360549
Status:
RECRUITING
Last Update Posted:
2024-04-11
First Post:
2024-04-06
Brief Title:
Effect of Percutaneous Acupoint Electrical Stimulation on Delirium
Sponsor:
Qin Zhang
Organization:
Tongji Hospital
Study Overview
Official Title:
Effect of Percutaneous Acupoint Electrical Stimulation on Delirium After Thoracoscopic Pneumonectomy
Status:
RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is a multicenter prospective randomized controlled clinical trial that aims to observe the impact of Transcutaneous Electrical Acupoint Stimulation TEAS on plasma TKMMP3 in a randomized controlled setting The intervention group received percutaneous acupoint electrical stimulation whereas the control group underwent conventional treatment The primary objective is to enhance the management of postoperative delirium specifically focusing on the occurrence and severity of delirium following thoracoscopic pulmonary resection Additionally various perioperative inflammatory markers cognitive function recovery quality pain levels anxiety sleep patterns postoperative complications and overall hospital stay duration were monitored to elucidate the mechanisms through which percutaneous acupoint electrical stimulation improves postoperative delirium
Detailed Description:
Transcutaneous Electrical Acupoint Stimulation TEAS is a treatment method that combines acupuncture point theory of traditional Chinese medicine with physical electrical stimulation techniques It achieves the purpose of acupoint stimulation by applying a weak current to a specific part Compared with traditional acupuncture TEAS has the advantages of non-invasiveness safety portability and adjustability Intraoperative acupoint electrical stimulation has no effect on operation and monitoring
This multicenter prospective randomized controlled clinical trial aims to investigate the impact of Transcutaneous Electrical Acupoint Stimulation TEAS on postoperative delirium following thoracoscopic pulmonary resection The study design involves the randomized allocation of participants into two groups an intervention group receiving percutaneous acupoint electrical stimulation and a control group undergoing standard postoperative care
The intervention protocol includes the precise selection of acupoints for TEAS application parameters for electrical stimulation frequency of treatments and duration of intervention sessions Patients in the control group will receive conventional postoperative management without TEAS
Outcome measures will assess plasma TKMMP3 levels incidence and severity of postoperative delirium perioperative inflammatory markers cognitive function pain levels anxiety sleep patterns postoperative complications recovery quality and hospital stay duration Statistical analysis will employ appropriate methods to evaluate the effectiveness of TEAS in managing postoperative delirium
Overall this clinical trial seeks to contribute to the understanding of how TEAS may improve postoperative delirium management and patient outcomes following thoracoscopic pulmonary resection The Detailed Description provides a comprehensive overview of the study protocol without duplicating information presented elsewhere in the document
This multicenter prospective randomized controlled clinical trial aims to investigate the impact of Transcutaneous Electrical Acupoint Stimulation TEAS on postoperative delirium following thoracoscopic pulmonary resection The study design involves the randomized allocation of participants into two groups an intervention group receiving percutaneous acupoint electrical stimulation and a control group undergoing standard postoperative care
The intervention protocol includes the precise selection of acupoints for TEAS application parameters for electrical stimulation frequency of treatments and duration of intervention sessions Patients in the control group will receive conventional postoperative management without TEAS
Outcome measures will assess plasma TKMMP3 levels incidence and severity of postoperative delirium perioperative inflammatory markers cognitive function pain levels anxiety sleep patterns postoperative complications recovery quality and hospital stay duration Statistical analysis will employ appropriate methods to evaluate the effectiveness of TEAS in managing postoperative delirium
Overall this clinical trial seeks to contribute to the understanding of how TEAS may improve postoperative delirium management and patient outcomes following thoracoscopic pulmonary resection The Detailed Description provides a comprehensive overview of the study protocol without duplicating information presented elsewhere in the document
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None