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CompletedNCT07906626BMIUpdated Oct 30, 2026

Snakehead Fish Extract and Curcumin Co-Supplementation in Advanced Lung Cancer on Inflammation, Nutritional Status, and Quality of Life

An interventional study of Snakehead Fish Extract and Curcumin in Lung Cancer (NSCLC), sponsored by Universitas Sumatera Utara. Completed at 1 site in Indonesia. Open to participants aged 40 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Universitas Sumatera Utara · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 3 months after the study started (first participant enrolled Jul 2025, registered Oct 2026).
Updated Oct 30, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
40 Years to 60 Years
Sex
All
01

Study summary

Background: Patients with advanced lung cancer receiving systemic therapy often experience nutritional decline, systemic inflammation, and impaired quality of life. Channa striata extract and Curcumin may offer complementary nutritional and anti-inflammatory support, but clinical evidence for their combination is limited.

The goal of this clinical trial is to learn if combined Channa striata (snakehead fish) extract and curcumin supplementation works to improve nutritional status, inflammation, and quality of life in adults with advanced lung cancer receiving systemic therapy. The main questions it aims to answer are:

  • Does Channa striata extract plus curcumin co-supplementation raise body weight in participants with advanced lung cancer?
  • Does this co-supplementation lower inflammatory markers in these participants?
  • Does this co-supplementation improve health-related quality of life in these participants?

Researchers will compare participants taking Channa striata extract plus curcumin to participants taking a placebo (a look-alike capsule that contains no active ingredients) to see if the co-supplementation works.

Participants will:

  • Take Channa striata extract plus curcumin capsules or placebo capsules 3 times daily for 9 weeks alongside their standard systemic therapy
  • Have their body weight (kg), body mass index, and mid-upper arm circumference checked (cm)
  • Give blood samples to test inflammatory markers
  • Answer questionnaire questions about their health-related quality of life (QLQ -C30)
Read the detailed description

Patients with advanced lung cancer receiving systemic therapy frequently experience progressive weight loss, systemic inflammation, and impaired quality of life. Channa striata extract provides nutritional support rich in amino acids, while curcumin exerts anti-inflammatory properties. This study aims to evaluate whether the combination of Channa striata extract and curcumin as an adjunct to standard systemic therapy improves clinical and nutritional outcomes in adults with advanced lung cancer.

Participants receive either the combination supplement (3000 mg Channa striata extract and 300 mg curcumin daily) or a matching placebo for 9 weeks while continuing their standard systemic therapy. Clinical assessments are conducted at baseline and after 9 weeks to evaluate changes in body weight, nutritional status (body mass index and mid-upper arm circumference), systemic inflammatory markers (C-reactive protein, TNF-alpha, and IL-6), and health-related quality of life.

02

Conditions studied

  • Lung Cancer (NSCLC)

Keywords

  • lung cancer
  • Channa striata
  • Curcumin
  • Body Weight
  • Inflammation markers
  • Quality of Life
03

In context

Lung Neoplasms

5,422 studies on the registry are indexed under Lung Neoplasms; 1,346 are open to participants now.

This study's enrollment of 60 is close to the median of 60 across 3,656 interventional studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Universitas Sumatera Utara is the lead sponsor of 24 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patients with newly diagnosed non-small cell lung carcinoma
  2. Consuming a combination supplement containing snakehead fish extract and curcumin extract until the second cycle
  3. Aged 40-60 years
  4. No history of allergies to freshwater fish or snakehead fish
  5. No history of allergies to foods containing curcumin
  6. Willing to participate in the study

Exclusion criteria

Exclusion Criteria:

  1. Lung cancer with performance status > 4
  2. (Body Mass Index) \< 18.5
  3. Mid-Upper Arm Circumference (MUAC) \< 23.5
  4. Allergy to supplements consumed during the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    INTERVENTION

    Drug: Snakehead Fish Extract and Curcumin

Interventions

  • DrugSnakehead Fish Extract and Curcumin

    Participants in the intervention group received 2 capsules 3 times daily for 3 months (9 Weeks). Each capsule contained 500 mg of Channa striata extract and 50 mg of curcumin (Striatamin®; PT Mega Medica, Jakarta, Indonesia), providing a total daily dose of 3000 mg of C. striata extract and 300 mg of curcumin.

06

What researchers measure

Primary outcomes

  1. Change from baseline in body weight at 9 weeks

    Body weight is measured in kilograms (kg) using a calibrated digital health scale at baseline and after 9 weeks of intervention. The metric is calculated as the post-intervention value minus the baseline value.

    Time frame: Baseline and After 9 weeks

Secondary outcomes

  1. Change from baseline in serum C-reactive protein (CRP) levels at 9 weeks

    Serum CRP levels are measured from venous blood samples using enzyme-linked immunosorbent assay (ELISA) and expressed in milligrams per deciliter (mg/dL).

    Time frame: Baseline and After 9 weeks

  2. Change from baseline in serum tumor necrosis factor-alpha (TNF-alpha) levels at 9 weeks

    Serum TNF-alpha levels are measured from venous blood samples using enzyme-linked immunosorbent assay (ELISA) and expressed in picograms per milliliter (pg/mL).

    Time frame: Baseline and After 9 weeks

  3. Change from baseline in serum interleukin-6 (IL-6) levels at 9 weeks

    Serum IL-6 levels are measured from venous blood samples using enzyme-linked immunosorbent assay (ELISA) and expressed in picograms per milliliter (pg/mL).

    Time frame: Baseline and After 9 weeks

  4. Change from baseline in mid-upper arm circumference (MUAC) at 9 weeks

    MUAC is measured in centimeters (cm) on the relaxed left arm at the midpoint between the acromion and olecranon process using a non-elastic measuring tape.

    Time frame: Baseline and After 9 weeks

  5. Change from baseline in Body Mass Index (BMI) at 9 weeks

    BMI is calculated as body weight in kilograms divided by height in meters squared (kg/m²).

    Time frame: Baseline and After 9 weeks

  6. Change from baseline in EORTC QLQ-C30 functional scale scores at 9 weeks

    Evaluates physical, role, emotional, cognitive, and social functioning using the EORTC QLQ-C30. Scores range from 0 to 100, where a higher score indicates a higher/better level of functioning.

    Time frame: Baseline and After 9 weeks

  7. Change from baseline in EORTC QLQ-C30 symptom scale scores at 9 weeks

    Evaluates symptoms including fatigue, nausea and vomiting, pain, dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties. Scores range from 0 to 100, where a higher score indicates a higher level of symptoms or greater symptom burden.

    Time frame: Baseline and After 9 weeks

  8. Change from baseline in EORTC QLQ-C30 global health status score at 9 weeks

    Assessed using the Indonesian version of the EORTC QLQ-C30 questionnaire. Global health status scores range from 0 to 100, where a higher score represents a better overall quality of life and higher level of general health.

    Time frame: Baseline and After 9 weeks

07

Study locations

1 site
  • Universitas Sumatera Utara
    Medan, North Sumatra 20154, Indonesia
08

References and documents

Individual participant data

Plan to share: No — The individual participant data (IPD) will not be shared to protect patient privacy and maintain the confidentiality of medical records, as approved by the Health Research Ethics Committee

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jul 2025 to primary completion in Jul 2026, 12 months.

Of 864 non-industry interventional studies with no phase under Lung Neoplasms, half reached primary completion within 35 months of starting (the median), counting those still running; a quarter within 16 and three quarters within 68. This study's 12 months is below that.

Counting every sponsor, half of 915 studies reached it within 34 months; a quarter within 15 and three quarters within 67.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 15, 2026
First posted
Oct 30, 2026
StartActual
Jul 1, 2025
Primary completionActual
Jul 1, 2026
CompletionActual
Sep 1, 2026
Last update
Oct 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07906626
Lead sponsor
Universitas Sumatera Utara
Responsible party
Noni Novisari Soeroso (Professor of Pulmonology Head of Thoracic Oncology Division, Universitas Sumatera Utara) — Principal investigator
First posted
Oct 30, 2026
Start date
Jul 1, 2025
Primary completion
Jul 1, 2026
Completion
Sep 1, 2026
Last update
Oct 30, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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