Study on the efficacy and mechanism of auricular pressure pills combined with acupuncture for the prevention and treatment of postoperative intestinal paralysis

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300075983

Enrollment

Unknown

Registered

2023-09-21

Start date

2023-10-01

Completion date

Unknown

Last updated

2023-09-26

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

Conditions

postoperative intestinal paralysis

Interventions

Intervention group:auricular acupoint pressure pill combined with acupuncture

Control group:routine treatment

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age = 18 years; 2) Patients undergoing elective laparoscopic surgery; 3) Patients voluntarily participating in the trial and signing an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients with severe diseases combining cardiac, cerebral and pulmonary systems and patients with severe psychiatric and cognitive disorders; 2) Patients who are unable to co-operate with the completion of the research programme, including speech difficulties, infectious diseases and other medical histories.

Design outcomes

Primary

Measure	Time frame
Incidence of delayed postoperative intestinal paralysis;Time to first postoperative bowel movement;	—

Secondary

Measure	Time frame
Length of postoperative stay;abdominal pain;Degree of bloating;nausea and vomiting;Amount and timing of solid food intake;	—

Countries

China

Contacts

Public ContactLYU RUOYUN

Shanghai Tenth People's Hospital

Rubylry@163.com+86 136 4180 8033

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026