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Clinical Efficacy and Mechanism of Action of Spirulina in Patients with Functional Constipation

Clinical Efficacy and Mechanism of Action of Spirulina in Patients with Functional Constipation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125491
Enrollment
Unknown
Registered
2026-05-27
Start date
2026-05-27
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

constipation

Interventions

Spirulina group:Spirulina (1g per tablet, 1 tablet per dose, 3 times per day) induction period: 7 days
intervention period: 21 days
washout period: 14 days
take placebo (1g per tablet, 1 tablet per dose, 3 times per day) for 21 days.
Placebo group:Placebo (1g per tablet, 1 tablet per dose, 3 times a day) induction period: 7 days
washout period: 14 days. Take spirulina (1g per tablet, 1 tablet per dose, 3 times a day) for 21 days.

Sponsors

The Second Affiliated Hospital of Hainan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old, gender not restricted; 2. Meet the diagnostic criteria for functional constipation; 3. Agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Previous diseases that cause weakness, cognitive impairment, aphasia, mental disorders or other conditions that may affect the patient's cooperation; 2. History of malignant tumors, severe cardiovascular or cerebrovascular diseases or history of abdominal surgery; 3. Patients with unexplained abdominal pain, patients with galactosemia and hyperuricemia; 4. Pregnant women, women preparing for pregnancy or breastfeeding women; 5. Patients who used antibiotics or probiotic preparations within 1 month before treatment or during treatment that may affect the intestinal flora; 6. Patients who did not take spirulina regularly, those who experienced adverse reactions or those considered unsuitable by the researchers.

Design outcomes

Primary

MeasureTime frame
The frequency of completely spontaneous defecation per week;Symptom Rating Scale for Constipation Patients Score;Hamilton Anxiety Scale score;

Countries

China

Contacts

Public ContactFeihu Bai

The Second Affiliated Hospital of Hainan Medical University

baifeihu_hy@163.com+86 898 6680 2026

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026