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A clinical study of transcutaneous acupoint interference current therapy for patients with opioid-induced constipation

A clinical study of transcutaneous acupoint interference current therapy for patients with opioid-induced constipation

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15007105
Enrollment
Unknown
Registered
2015-09-08
Start date
2014-03-01
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

opioid-induced constipation

Interventions

Two groups:transcutaneous acupoint interference current therapy versus control

Sponsors

234 Gucui Road, Hangzhou, Zhejiang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. patients recieve analgesic therapy with daily uge of oxycodone hydrochloride delayed release tablets >=80 mg; 2. those who meet the diagnostic criteria of rome ? for constipation; 3. those aged between 18 80 years old; 4. those no other management for constipation during 2 weeks before enrollment except rescue symptomatic treatment for acute intestinal obstruction gas; 5. those who have no language barrier signed informed consents.

Exclusion criteria

Exclusion criteria: 1. patients with other secondary constipation caused by metabolic, endocrine, nervous, postoperative diseases or intestinal organic diseases (such as crohns disease, intestinal tuberculosis, etc.); 2. those who accompanied by serious cardiovascular, hepatic, renal, or psychiatric diseases, influencing the cooperation, examination or follow-up process of taifc; 3. pregnant or lactating women.

Design outcomes

Secondary

MeasureTime frame
numeric rating scales;patient assessment of constipation quality of life;

Primary

MeasureTime frame
cleavelconstipation scales;

Countries

China

Contacts

Public ContactHuadong Zhu
yuhaineurosg@126.com+86 15088502150

Outcome results

None listed

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