Clinical trial · Observational
Pilot Observational Study and Safety Analysis of FL Nourish Capsules in Cancer Patients in Remission
NCT06807515CI-TRIAL-00088367enrolling by invitationClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a single-centre, observational prospective study of cancer patients in remission administering FL Nourish capsules (FLNC), a proprietary Chinese Medicine herbal supplement, for the treatment of symptoms associated with qi deficiency and blood stasis syndrome.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Cancer Survivor | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (1)
- label
- FLNC Group
Primary outcomes (1)
- measure
- Pre-post values of EORTC QLQ-C30 questionnaire test scores
- timeFrame
- From enrollment to the end of treatment at 10 months
- description
- 0 is equivalent to a low QoL/functioning/symptom score and 100 indicates the best posssible QoL/functioning/symptom score.
Secondary outcomes (4)
- measure
- Incidence of unanticipated adverse events or severe adverse events: estimated to be <= 10%
- timeFrame
- From enrollment to the end of treatment at 10 months
- measure
- Pre-post values of Alanine aminotransferase (ALT)
- timeFrame
- From enrollment to the end of treatment at 10 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Aged 21-80; * Cancer diagnosis ≤ 5 years; * Received treatment with no current evidence of recurrence, with predicted life expectancy of 12 months and above; * On regular follow-up with lab tests scheduled every 1-9 months; * Recent (\<=3 months) blood test report(s) available on first study visit * Diagnosed with the TCM syndrome of Qi deficiency and Blood stasis by the primary physician: experience 2 major symptoms coupled with typical tongue and pulse conditions; 2 major symptoms and 1 possible symptom coupled with tongue and pulse conditions; and 1 major symptom and at least 2 possible symptoms coupled with tongue and pulse conditions; Exclusion Criteria: * On active cancer treatment such as IV chemotherapy or radiotherapy or oral targeted therapy (excluding HRT and oral chemotherapy); * Scheduled for IV chemotherapy, radiotherapy or surgery within the next 1 year from recruitment date; * Diagnosed with active disease of the liver, kidney, brain, blood, blood vessels; with mental health conditions or are mentally incapacitated; * Pregnant women.
References
Publications (1)
- BACKGROUNDChan A, Chan D, Ng DQ, Zheng HF, Tan QM, Tan CJ, Toh JHM, Yap NY, Toh YL, Ke Y, Wang ECA, Lim QPN, Ho HK, Chew L, Tan TJ. HEalth-Related Quality of Life-Intervention in Survivors of Breast and Other Cancers Experiencing Cancer-Related Fatigue and Associated Cognitive Symptoms Using TraditionAL Chinese Medicine: The 'HERBAL' Trial. Integr Cancer Ther. 2025 Jan-Dec;24:15347354251314514. doi: 10.1177/15347354251314514. PMID 39840742