Clinical Trials · PAR-EQ-B
Sample Size for an Equivalence Trial with a Binary Outcome
Use this calculator to plan a two-arm equivalence trial with a binary outcome when clinically acceptable differences are defined by symmetric absolute risk-difference limits.
4. Results
Enter the trial assumptions and select Calculate.
Suggested sample-size wording
Warnings
Formula, assumptions, limitations, and methodological note
Example clinical scenario
A randomized trial compares clinical-response proportions for a generic treatment and its reference product and is designed to show equivalence within prespecified margins.
Formula and methodological note
This calculator uses the specified Chow et al. large-sample normal-approximation method for two independent parallel groups. It assumes the planned allocation ratio, no clustering or pairing, and no covariate adjustment. It does not implement exact, score-based, Farrington–Manning, crossover, repeated-measures, or cluster-trial methods.
The equivalence calculation uses a conservative symmetric-margin formula. With a 5% alpha for each one-sided test, its confidence-interval interpretation uses a 90% two-sided confidence interval.
Technical results
Method references
- Chow SC, Shao J, Wang H, Lokhnygina Y. Sample Size Calculations in Clinical Research. 3rd ed. CRC Press; 2018. Eq. 4.9.
Suggested citation
Yaacob, Najib Majdi. “Sample Size for an Equivalence Trial with a Binary Outcome (PAR-EQ-B).” Web calculator. NajibMY, 2026. Accessed July 29, 2026. http://127.0.0.1:4321/tools/sample-size/clinical-complex-study-designs/equivalence-binary-outcome/.