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Clinical study on the prevention and treatment of gastrointestinal dysfunction after lumbar internal fixation by percutaneous acupoint electrical stimulation

Clinical study on the prevention and treatment of gastrointestinal dysfunction after lumbar internal fixation by percutaneous acupoint electrical stimulation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005798
Enrollment
Unknown
Registered
2022-04-03
Start date
2022-04-06
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative gastrointestinal dysfunction

Interventions

Experimental group :2 hours after surgery, percutaneous acupoint electrical stimulation was performed for 30 minutes (2/100Hz dense wave)
Control group :Two hours after the operation, pseudo-percutaneous acupuncture point electrical stimulation was performed for 30 minutes

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion 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

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.

Design outcomes

Primary

MeasureTime frame
Time of first anal exhaust after surgery;

Secondary

MeasureTime frame
The incidence of adverse reactions to percutaneous acupoint electrical stimulation;Gastrin;Interleukin-6;Recovery time of bowel sounds;Postoperative nausea and vomiting;Tumor necrosis factor -a;Postoperative abdominal distension;Motilin;Time of first postoperative anal defecation;Time of oral solid food intake (and intolerance);Vasoactive intestinal peptide;

Countries

China

Contacts

Public ContactXu Huiqing

Wangjing Hospital, China Academy of Chinese Medical Sciences

dr_xuhuiqing@sina.com13683395622

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026