Asafoetida and indigestion

What 2 graded rows on asafoetida agree on for indigestion, and where they differ. Counted side by side, never averaged.

What the rows agree on

Each block and row is one graded row from the Asafoetida page, with its PubMed record.

Your question

Supplement
Asafoetida Choose another

Asafoetida and indigestion

2 rows · 105 people

They agree: both rows found an improvement.

No difference
Improved
Each block is one evidence row, sized by how many people it enrolled, with its grade inside.
  • Grade C× 2
Rows
2
Trials
2
People
105

What the rows share

From the rows

The best-graded row, grade C, is a randomized trial of 62 people (2025) and found an improvement.

The rows run from 43 to 62 people, published from 2018 to 2025: 2 single studies.

The rows

2 improved
  1. Grade CFunctional dyspepsia symptoms (early satiety, bloating, heartburn) · Improved

    RCT · n 62 · 2025 · Adults with functional dyspepsia symptoms

    250 mg/day · 14 days

    Significant time, treatment and treatment × time effects for early satiety, bloating and heartburn (P < .05), with more responders by day 14. Stool form improved, reaction time fell 44% and Bergen Insomnia Scale scores improved (both P < .001).

    Row on the Asafoetida page · PubMed 41054174 (opens PubMed)

  2. Grade CFunctional dyspepsia symptoms and quality of life · Improved

    RCT · n 43 · 2018 · People with moderate to severe functional (non-ulcer) dyspepsia in India

    250 mg twice daily (500 mg/day) · 30 days

    About 81% of the asafoetida group improved significantly in overall score and quality of life versus placebo (p < 0.01), and 66% were symptom-free at the end. Symptom scores improved in both groups but more with asafoetida (−5.67 to −25.29 vs −1.55 to −6.0; p ≤ 0.001). No adverse events or blood-test changes occurred.

    Row on the Asafoetida page · PubMed 30224930 (opens PubMed)

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