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Effect of acupuncture on hormone level in patients with gastrointestinal dysfunction after general anesthesia

Effect of acupuncture on hormone level in patients with gastrointestinal dysfunction after general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016991
Enrollment
Unknown
Registered
2018-07-06
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-07-09

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

Conditions

Gastrointestinal dysfunction after general anesthesia

Interventions

Acupuncture group:Acupuncture group
The control group:granisetron

Sponsors

Mianyang Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. General anesthesia; 2. Postoperative compliance with laparoscopic surgery, etc.; And ASA grade I--II; 3. Weight 45kg to 75kg, BMI 18.5 to 26; 4. Operation time: 2+1.0h; 5. Aged 18 to 70 years old; 6. Subjects are informed and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Obese pregnancy, lactation, or within 3 months with a fertility or fertility plan; 2. Patients with severe heart, liver, kidney, lung and hematopoietic system diseases, central nervous system diseases and mental disorders; 3. Patients were treated with anti-vomiting drugs within 24h before surgery, and gastric tube was retained after surgery; 4. I have a history of gastrointestinal surgery, and now I have bleeding from acute gastroenteritis or active gastrointestinal ulcer; 5. The anesthesia was non-general anesthesia, with ASA grading greater than or equal to grade III, and operation time >180min; 6. Patients with aversion to acupuncture treatment, poor compliance, or aphasia, audio-visual impairment; 7. Patients who have participated in other clinical trials within one month; 8. Intraoperative blood loss is greater than or equal to 1000ml or hemoglobin <70g/L; 9. Other situations that the researchers considered inappropriate for inclusion; If the patient satisfies any of the above, the patient is not eligible to participate in this study.

Design outcomes

Primary

MeasureTime frame
Gastric secrete element;Serum motilin;Serum ghrelin;Serum serotonin;

Secondary

MeasureTime frame
Nausea and vomiting;The degree of abdominal distension;Number of bowel;Postoperative first bowel movement time;Postoperative first exhaust time;

Countries

China

Contacts

Public ContactXiu-li Yuan

Mianyang Traditional Chinese Medicine Hospital

573859636@qq.com+86 18990170303

Outcome results

None listed

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