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Acupuncture Therapy for Post-Stroke Constipation: A Randomized Clinical Trial

Acupuncture Therapy for Post-Stroke Constipation: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001499
Enrollment
Unknown
Registered
2026-06-17
Start date
2026-06-23
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Functional constipation

Interventions

Drug group:Routine drug therapy
Acupuncture group:Acupuncture
Drug and Acupuncture Combined Therapy Group:Routine medications combined with acupuncture therapy

Sponsors

Fujian Province Nanping City First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18–80 years; (2) Confirmed diagnosis of stroke (ischemic or hemorrhagic) by CT or MRI; (3) Post-stroke constipation meeting Rome IV criteria for functional constipation; (4) Within 2 weeks to 6 months after stroke onset; (5) Glasgow Coma Scale score =7 points; (6) No history of constipation prior to stroke, with constipation symptoms persisting for at least 2 weeks post-stroke; (7) Ability to follow the intervention protocol and signed informed consent from the patient or their legal representative.

Exclusion criteria

Exclusion criteria: (1) History of severe organic diseases of the digestive tract (such as intestinal obstruction, intestinal tumors, inflammatory bowel disease, etc.); (2) Severe dysfunction of heart, liver, or kidney, or other severe systemic diseases that may affect safety or tolerance to the intervention; (3) Pregnant or breastfeeding women; (4) History of regular acupuncture treatment to improve constipation, to avoid confounding of intervention effects; (5) Severe impairment of cognitive function, unable to understand or complete assessment scales and intervention requirements; (6) Other situations deemed unsuitable for participation in clinical trials, as judged by the study physician, which may affect safety or compliance.

Design outcomes

Primary

MeasureTime frame
Weekly spontaneous bowel movements;

Secondary

MeasureTime frame
Constipation Scoring System;Bristol Stool Scale;Patient Constipation Symptom Assessment;Overall Quality of Life for Stroke Patients (SS-QOL);

Countries

China

Contacts

Public ContactXin Zhang

Nanping First Hospital

zx1290289847@163.com15735641668

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026