ITMCTR2200005798
Not yet recruiting
Phase 1
Clinical study on the prevention and treatment of gastrointestinal dysfunction after lumbar internal fixation by percutaneous acupoint electrical stimulation
Wangjing Hospital, China Academy of Chinese Medical Sciences0 sitesTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Postoperative gastrointestinal dysfunction
- Sponsor
- Wangjing Hospital, China Academy of Chinese Medical Sciences
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(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.
Exclusion Criteria
- •(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.
Outcomes
Primary Outcomes
Not specified
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