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Butyrate Yogurt for Cancer Constipation

A Phase II Study on the Efficacy and Safety of Butyrate-Containing Short-Chain Fatty Acid Yogurt in Constipation in Patients With Gastrointestinal Malignancies

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07723729
Enrollment
30
Registered
2026-07-23
Start date
2026-08-01
Completion date
2027-12-30
Last updated
2026-07-23

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

Conditions

Constipation, Gastrointestinal Cancer

Brief summary

Constipation is a common yet underrecognized supportive care issue in cancer patients. Its consequences extend beyond physical discomfort to include impaired quality of life, reduced opioid adherence leading to inadequate analgesia, and increased risks of fecal impaction, emergency visits, and hospitalization. Current management strategies-including laxatives, stool softeners, prokinetics, and PAMORAs-remain suboptimal due to limited effects on gut dysbiosis, mucosal barrier dysfunction, and chronic inflammation, as well as issues related to polypharmacy, variable efficacy, and long-term tolerability. Hence, there is a clear need for novel, well-tolerated, long-term interventions with nutritional benefits that target the gut microbiota-mucosal barrier-motility axis. Short-chain fatty acids (SCFAs), particularly butyrate, are key microbial metabolites that may improve constipation through multiple mechanisms: enhancing intestinal motility via enteric nervous system regulation, reinforcing mucosal barrier integrity and mitigating low-grade inflammation, and restoring gut microbial-metabolite homeostasis. Butyrate supplementation therefore holds mechanistic promise for cancer-related constipation. The "Small Blue Can High Dietary Fiber Butyrate SCFA Yogurt" (Blueglass) is designed with a "probiotics + prebiotics + acids" synergistic fermentation platform, delivering ≥70 mg/100 g butyrate combined with high dietary fiber. Compared with conventional laxatives or single-agent butyrate, this yogurt-based formulation offers potential advantages in patient acceptability, long-term adherence, dual exogenous and endogenous SCFA support, and multi-target action on motility, microbiome, and barrier function, making it a promising candidate for supportive care in this population.

Interventions

DIETARY_SUPPLEMENTbutyrate-containing short-chain fatty acid yogurt

Eligible constipated patients were treated with butyrate-containing short-chain fatty acid yogurt

Sponsors

Tianjin Medical University Cancer Institute and Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years. 2. Histologically confirmed diagnosis of gastrointestinal malignancy. 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2. 4. Confirmed \< 3 spontaneous bowel movements (CSBM) per week during the 1-week baseline period, accompanied by constipation-related symptoms (e.g., straining, hard/lumpy stools, sensation of incomplete evacuation, etc.). 5. Anticancer treatment regimen is expected to remain relatively stable during the study period. 6. Willing and able to provide written informed consent and complete electronic diary entries.

Exclusion criteria

1. Mechanical intestinal obstruction, active inflammatory bowel disease, severe rectal stricture, or acute abdomen. 2. Absolute neutrophil count (ANC) \< 1.0 × 10⁹/L or active infection. 3. New initiation or major dose adjustment of prosecretory or prokinetic agents within the past 2 weeks. 4. Allergy or hypersensitivity to dairy products or any component of the butyrate-containing yogurt formulation. 5. Deemed unsuitable for enrollment by the investigator (e.g., poor compliance, cognitive impairment, or other conditions that may interfere with study participation).

Design outcomes

Primary

MeasureTime frame
Efficacy rate for constipationFrom enrollment to the end of treatment at 6 weeks

Contacts

CONTACTTao Ning
ningtao37@163.com+8613821828358

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 24, 2026