Gastrointestinal Dysfunction
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) must be aged 18 to 65 years; 2) selective operation on laparoscopic surgery anesthesia; 3) have no experience of intradermal needling before this study; 4) are not involved in any other clinical trials during the same period; 5) do not have cognitive impairment, aphasia, or mental disorders, thereby possessing unimpaired communication ability, and can understand and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1) are pregnant or lactating; 2) have a history of abdominal surgery; 3) have undergone more procedures than LC alone as part of their treatment; 4) have sustained damage to the selected acupoints; 5) have an allergy to the adhesive; 6) suffer from severe gastrointestinal or chronic pain disorders (such as chronic pelvic pain), and have taken analgesic drugs during the past 48 hor over a long period of time; 7) have a serious disease of the heart, brain, liver, kidney, or hematopoietic system; 8) have a history of drug abuse (e.g., morphine), motor-induced or surgery-induced vomiting, obesity (body weight > 80 kg), diabetes, or are bedridden.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| first passage of flatus; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to first defecation;Abdominal pain;Abdominal distention;Nausea;Vomit;Blood Gerhlin;The hospital anxiety depression scale (HADS);the Gastrointestinal Quality of Life Index,GIQLI; | — |
Countries
China
Contacts
Tianjin Nankai Hospital