Status:
UNKNOWN
Patients Undergoing Laparoscopic Radical Gastrectomy Walk Out From Operating Room After Surgery ( WOFOR-G-01 )
Lead Sponsor:
Sixth Affiliated Hospital, Sun Yat-sen University
Conditions:
Laparoscopic Radical Gastrectomy
Enhanced Recovery After Surgery
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
Although early and progressive mobility is widely accepted as an important aspect of postoperative care, guidelines and recommendations suggesting the exact timing and intensity of mobilization effort...
Detailed Description
Postoperative bed rest increases the risk of complications such as thromboembolism and intestinal adhesion, but actual clinical effects of early mobilization still need randomized control trails to pr...
Eligibility Criteria
Inclusion
- Age 18-65 Years old
- scheduled for laparoscopic radical gastrectomy.
- American Society of Anesthesiologists (ASA) grading I or II
Exclusion
- Patients have severe cardiac diseases (cardiac function grading greater than grade 3/arrhythmia including sick sinus syndrome, atrial fibrillation, atrial flutter, atrioventricular block, frequent ventricular premature,multiple ventricular premature, ventricular premature R on T, ventricular fibrillation and ventricular flutter/acute coronary syndrome) or respiratory failure or hepatic failure or renal failure;
- Body mass index (BMI) ≥30 kg/m2;
- Preoperative hemoglobin\<80 g/L or albumin\<30 g/L
- Patients have diabetics or patients with gastric emptying disorders;
- Patients with poor blood pressure control (receive regular antihypertensive medical treatment but still have systolic blood pressure\>150 mmHg and/or diastolic blood pressure\>90 mmHg );
- Patients have schizophrenia, epilepsy, Parkinson's disease, mental retardation, or hearing impairment.
- Patients have thrombosis such as in lower extremity or in vena cava or in other veins.
- Patients have neuromuscular disorders affecting lower limb activity, such as myasthenia gravis and cerebral infarction, which cause lower limb muscle weakness;
- Patients have contraindications for epidural puncture.
- Postoperative placement of drainage tube for coelom hyperthermia perfusion
- Patients participate in other clinical trials.
- Patients refuse to sign informed consent for research.
Key Trial Info
Start Date :
August 27 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 30 2024
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT04029753
Start Date
August 27 2019
End Date
December 30 2024
Last Update
November 1 2022
Active Locations (1)
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1
the Sixth Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China, 510655