Effects of abdominal moxibustion on postoperative gastrointestinal function recovery and intestinal microflora of patients undergoing spinal surgery

Phase 1

• Conditions: postoperative period

• Registration Number: ITMCTR2100005463
• Lead Sponsor: GuangDong Provincial Hospital of Chinese Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

1. Patients undergoing elective spinal surgery under endotracheal general anesthesia;
2. Age 18-65;
3. American Society of Anesthesiologists (ASA) grade ? - ?;
4. The patient had fully understood the study and voluntarily signed a written informed consent before the study began.

Exclusion Criteria

1. Those who are allergic to moxibustion and resistant to moxibustion cannot be treated or those who are unable to perform moxibustion due to diseases existing in the surface area of acupoints involved in this study;
2. Preoperative conscious cognitive, visual and auditory impairment or doctor-patient communication difficulties, unable to complete gastrointestinal function measurement;
3. Patients with intestinal functional organic lesions;
4. Diabetes, hyperthyroidism and hypoimmune deficiency intestinal parasitic diseases with severe hypoproteinemia (albumin & LT; 30g/L) severe electrolyte disturbances such as hypokalemia (blood K+< 2.5mmol/L) traumatic T6 and below fracture may cause visceral motor nerve injury;
5. A large number of hormones or non-steroidal anti-inflammatory agents were used in the last 2 weeks to affect electrolyte metabolism;
6. Patients who were simultaneously treated preoperatively with drugs that affected the efficacy evaluation of this study (such as Smecta, dexide, cisapride, etc.);
7. Previous history of schizophrenia, Parkinson's disease or epilepsy;
8. Refused to participate in this experiment.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The time to the first defecation after surgery;The time to the first passage of flatus after surgery;The time to first Bowel sound recovery;

Secondary Outcome Measures

Name	Time	Method
GSRS;Identification of intestinal flora;Inflammatory markers and nutritional status assessment;