Clinical randomized controlled trial of electric acupuncture treatment of severe acute pancreatitis paralytic ileus

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-13003165

Enrollment

Unknown

Registered

2013-01-29

Start date

2013-01-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

severe acute pancreatitis paralytic ileus

Interventions

Acupuncture group:SJ6 and S36 at both sides is punctured perpendicularly 2—3cm then connect ipsilateral SJ6 and S36 with the 6805 - D electric acupuncture apparatus, which produced by santou medical e

Sham-acupuncture control group:Sham point at both sides is punctured perpendicularly 2-3cm, then exit to skin, connect the sham point ipsilateral with the 6805 - D electric acupuncture apparatus which

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Accord with severe acute pancreatitis diagnosis standard(Revision of the standard in 2001 the Chinese Medical Association of pancreatic surgery "The draft principles of diagnosis and treatment of severe acute pancreatitis"); 2. All the patients anal stop exhaust (or) bowel movement more than 24 h, and accompanied by clear abdominal symptoms,including: obviously tenderness, bounce pain,muscle tension, abdominal distension, bowel sound reduced (< 3 times/min) or disappear (0 time / 3-5 min); 3. Aged 18- 65 years old; 4. informed consent signedVolunteered to participate in the study.

Exclusion criteria

Exclusion criteria: 1. therapeutic eliminate acute abdominal pain and low potassium, anesthesia, mechanical factors caused by intestinal paralysis and gastric ulcer, such as mechanical damage caused by stomach bleeding and oral bleeding, haemoptysis, etc; 2. with a serious heart, liver and kidney damage, the blood system primary disease or cognitive dysfunction, aphasia, mental disorder, or unable to coordinate with the inspection and healers; 3. the pregnancy or lactation patients; 4. the installation of cardiac pacemaker.

Design outcomes

Primary

Measure	Time frame
The anus exhaust time;For the first time defecation time;First time eating solid food;Transit number surgery patient;	—

Secondary

Measure	Time frame
Abdominal pain score;Abdominal distension disappear time;Blood amylase, blood calcium returned to normal time;	—

Countries

China

Contacts

Public ContactLi Ning/Li Jia

zhenjiuhuaxi@163.com+86 18980601617

Outcome results

None listed

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