Clinical study on the prevention and treatment of gastrointestinal dysfunction after lumbar internal fixation by percutaneous acupoint electrical stimulatio
- Conditions
- Postoperative gastrointestinal dysfunction
- Registration Number
- ITMCTR2200005798
- Lead Sponsor
- Wangjing Hospital, China Academy of Chinese Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
(1) Surgical treatment of lumbar internal fixation under general anesthesia should be performed at an appropriate time.
(2) American Society of Anesthesiologists (ASA) Grade I-II.
(3) Between the ages of 18 and 65.
(4) Normal oral diet, normal exhaust and defecation, and no other serious gastrointestinal diseases before surgery.
(5) Good communication skills, able to fully understand and cooperate in completing CRF evaluation.
(6) Signed informed consent and volunteered to participate in this study.
(1)Patients with contraindications to percutaneous electrical stimulation, including stimulated local skin injury or infection, implanted electrophysiological devices.
(2) serious dysfunction of heart, brain, lung, liver, kidney and other important system organs.
(3) Communication disorders, including language disorders, previous neurological diseases and mental disorders.
(4) Severe obesity (BMI>30kg/m2) or severe malnutrition.
(5) Long-term use of sedatives, drugs.
(6) Erecstool dysfunction caused by severe spinal cord injury or cauda equina nerve injury.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method