Clinical Trials · PAR-NI-C
Sample Size for a Non-Inferiority Trial with a Continuous Outcome
Use this calculator to plan a two-arm non-inferiority trial with a continuous primary outcome when the maximum acceptable loss relative to the active control is prespecified.
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 change in lung-function score between a simpler inhaler and standard therapy and is designed to exclude a clinically unacceptable loss of benefit.
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.
Technical results
Method references
- Chow SC, Shao J, Wang H, Lokhnygina Y. Sample Size Calculations in Clinical Research. 3rd ed. CRC Press; 2018. Eq. 3.12.
Suggested citation
Yaacob, Najib Majdi. “Sample Size for a Non-Inferiority Trial with a Continuous Outcome (PAR-NI-C).” Web calculator. NajibMY, 2026. Accessed July 29, 2026. http://127.0.0.1:4321/tools/sample-size/clinical-complex-study-designs/non-inferiority-continuous-outcome/.