Actively Recruiting
Patients Undergoing Laparoscopic Colorectal Surgery Walk Out From Operating Room After Surgery ( WOFOR-C1 )
Led by Sixth Affiliated Hospital, Sun Yat-sen University · Updated on 2024-07-08
300
Participants Needed
1
Research Sites
265 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Early mobilization is considered as an important strategy to enhance postoperative recovery. However, direct association between very early mobilization and improved recovery needs randomized control trials to prove. This study proposes the program of walking out from operating room (WOFOR) after surgery, which means that encouraging patients to walk out from the operating room and return to the ward by walking under the condition of painlessness, clear consciousness and normal muscle strength of lower limb. The aim of this randomized controlled trial is to investigate the effect of WOFOR on the postoperative recovery of patients undergoing laparoscopic colorectal surgery.
CONDITIONS
Official Title
Patients Undergoing Laparoscopic Colorectal Surgery Walk Out From Operating Room After Surgery ( WOFOR-C1 )
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-65 years
- Scheduled for laparoscopic colectomy or laparoscopic rectectomy surgery (Dixon technique)
- American Society of Anesthesiology grade I or II
You will not qualify if you...
- Severe cardiac diseases including cardiac function grade greater than 3 or arrhythmias such as sick sinus syndrome, atrial fibrillation, atrial flutter, atrioventricular block, frequent ventricular premature beats, ventricular fibrillation, or ventricular flutter
- Respiratory failure, hepatic failure, or renal failure
- Poor blood glucose control with glycosylated hemoglobin over 7%
- Poor blood pressure control with systolic pressure above 150 mmHg and/or diastolic pressure above 90 mmHg despite regular antihypertensive treatment
- Schizophrenia, epilepsy, Parkinson's disease, mental retardation, or hearing impairment
- Presence of thrombosis in lower extremities or other veins
- Neuromuscular disorders affecting lower limb activity such as myasthenia gravis or cerebral infarction causing muscle weakness
- Contraindications for epidural puncture
- Refusal to sign informed consent for research
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
the Sixth Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China, 510655
Actively Recruiting
Research Team
S
SanQing Jin, MD
CONTACT
Y
Yang Zhao, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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