Actively Recruiting
A Study of the Association Between Frailty and Acute Postoperative Pain in Elderly Thoracoscopic Surgery Patients
Led by Huazhong University of Science and Technology · Updated on 2024-06-21
78
Participants Needed
1
Research Sites
33 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To gain a clearer understanding of the association between frailty and postoperative acute pain in elderly thoracoscopic surgery patients and its underlying mechanisms, to provide new solution ideas to reduce the level of postoperative acute pain and improve the debilitating state of elderly thoracoscopic surgery patients, and consequently improve their quality of life and mental status.
CONDITIONS
Official Title
A Study of the Association Between Frailty and Acute Postoperative Pain in Elderly Thoracoscopic Surgery Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing thoracic surgery under general anesthesia with 48 hours of postoperative patient-controlled analgesia
- Age 60 years or older
- ASA class I-III
- Signed informed consent
- Patients undergoing thoracoscopic surgery
You will not qualify if you...
- Patients who refuse to participate in the study
- Drug dependence
- Patients with verbal communication difficulties or inability to cooperate
- Patients unable to assess frailty preoperatively or pain postoperatively
- Failure to provide a compliant fecal sample at the agreed time
- Antibiotic treatment within the last month
- Intestinal dysfunction such as irritable bowel syndrome, inflammatory bowel disease, or chronic diarrhea
- Comorbid metabolic disorders that may affect the microbial community, such as thyroid dysfunction or diabetes mellitus
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China, 430030
Actively Recruiting
Research Team
X
Xianwei Zhang, Doctor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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