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Different dosage regimens of Konjac Tong for improving intestinal function in cancer patients undergoing radiotherapy or chemotherapy: a multicenter, prospective, randomized controlled trial

Different dosage regimens of Konjac Tong for improving intestinal function in cancer patients undergoing radiotherapy or chemotherapy: a multicenter, prospective, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123428
Enrollment
Unknown
Registered
2026-04-27
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Malignant neoplasm (confirmed by pathology)

Interventions

Intervention Group 1 (Group B):On the basis of routine care, take 1 sachet (10 g) of Konjac Tong product per day for three consecutive weeks.
Intervention Group 2 (Group C): On the basis of routine care, take 2 sachets (20 g) of Konjac Tong product per day for three consecutive weeks.
Blank Control Group (Group A) – Routine Care::Routine Care:After admission, provide both verbal and written information to patients and their families about the causes, common complications, and preve
instruct patients or their caregivers to learn and perform clockwise abdominal massage to assist in promoting intestinal peristalsis. During diarrhea-prone periods, recommend a low-fiber, easily diges

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age >= 18 years; (2) Patients with pathologically confirmed malignant tumors who are receiving radiotherapy, chemotherapy, or concurrent chemoradiotherapy; (3) Occurrence of constipation and/or diarrhea during radiotherapy/chemotherapy. Constipation is defined according to Rome IV criteria: spontaneous bowel movements (SBM) 3 times per day) compared with usual habit, loose or watery stools (BSFS type 5–7), increased water content (>85%), possibly accompanied by mucus, pus, blood, or undigested food; (4) Expected survival >= 3 months; (5) Normal cognitive and expressive abilities; (6) Voluntarily agree to participate in the study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergy to konjac or its derivative components; 2. Concurrent inflammatory bowel disease, Crohn's disease, or other intestinal disorders; 3. Recent use of potent laxatives (e.g., stimulant laxatives) that cannot be discontinued; 4. Mental disorders or long-term use of psychotropic medications; 5. Cognitive impairment or inability to comply with the study procedures.

Design outcomes

Primary

MeasureTime frame
Assessment of intestinal function;Improvement of constipation symptoms;

Secondary

MeasureTime frame
Improvement of sleep quality;Quality of life of cancer patients;

Countries

China

Contacts

Public ContactHu hai

Sichuan Cancer Hospital

Hu_hai2019@outlook.com+86 135 4066 2185

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026