Clinical Trials Directory

Trials / Unknown

UnknownNCT04516174

Effect of Transversus Abdominis Plane Block Combined With Dexmedetomidine Infusion on the Prognosis in Elderly Patients Undergoing Abdominal Surgery

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
180 (estimated)
Sponsor
Beijing Tiantan Hospital · Academic / Other
Sex
All
Age
65 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To compare the prognosis of elderly patients undergoing radical resection of colorectal cancer treated with general anesthesia and general anesthesia combined with transversus abdominis plane block and continuous infusion of dexmedetomidine. The incidence of postoperative delirium, postoperative acute pain moderately to severely and poor postoperative recovery were composite endpoints to determine the prognosis of patients.

Conditions

Interventions

TypeNameDescription
PROCEDURETransversus abdominis plane block using ropivacaineBefore anesthesia, the ultrasound-guided bilateral transversus abdominis plane block using 0.25% ropivacaine was perdormed by anesthesiologist who is not involved in intraoperative management and postoperative follow-up and evaluate the effect after the block completed.
DRUGDexmedetomidineAfter finished the transversus abdominis plane block, then perform tracheal intubation and start the infusion of dexmedetomidine.
PROCEDURETransversus abdominis plane block using salineBefore anesthesia, the ultrasound-guided bilateral transversus abdominis plane block using saline was perdormed by anesthesiologist who is not involved in intraoperative management and postoperative follow-up and evaluate the effect after the block completed.
DRUGSalineAfter finished the transversus abdominis plane block, then perform tracheal intubation and start the infusion of saline, dosage and infusion method of saline are consistent with dexmedetomidine.

Timeline

Start date
2020-09-01
Primary completion
2022-12-31
Completion
2023-09-01
First posted
2020-08-18
Last updated
2020-08-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04516174. Inclusion in this directory is not an endorsement.