Related Experiment Video
Updated: Jun 6, 2025

Optimizing the Modified No-Scalpel Vasectomy Technique
Published on: October 18, 2024
Impact of prednisone on vasectomy reversal outcomes (iPRED study): results from a randomized, controlled clinical
Landon Trost1, Sevann Helo2, Klinton Brearton3
1Male Fertility and Peyronie's Clinic, Orem, Utah; Department of Physiology and Developmental Biology, Brigham Young University, Provo, Utah.
Objective:
To evaluate the safety and efficacy of prednisone on pregnancy rates and semen concentrations at 1 year after vasectomy reversal.
Design:
Randomized, controlled trial (NCT04788823).
Subjects:
Men undergoing vasectomy reversal.
Intervention:
Participants were randomly assigned 1:1:1:1 to Control (no prednisone), Pred High (20 mg prednisone taper, every other month × 3 months), Pred PRN (20 mg prednisone taper × 3 courses maximum if sperm counts were declining or 0), and Pred Low (5 mg/d, every other week × 6 months). Note that Pred High and Pred PRN were stopped prematurely due to interim findings demonstrating lower pregnancy rates.
Main Outcome Measures:
Pregnancy rates, semen concentrations, and adverse events. The current study reports outcomes at 1 year.
Results:
A total of 75 men were enrolled, with 1-year data available in 73 (Control, n = 25; Pred High, n = 14; Pred PRN, n = 11; and Pred Low, n = 23). Baseline factors were similar among cohorts. Pregnancy rates at 12 months were higher in Controls (65%) and Pred Low (67%) compared with Pred High (17%) and Pred PRN (38%). Overall patency at 12 months (sperm at any point) was 99%, with no statistically significant differences noted between groups for patency, median concentrations by month (range, 3-42), or overall median concentrations (median of medians range, 5-16).
Conclusion:
High-dose (20 mg) prednisone results in decreased pregnancy rates after vasectomy reversal, an effect which is independent of sperm concentration, dose dependent, and persists for months after discontinuation. Prednisone doses (ranging from 5 to 20 mg) do not impact sperm concentrations.
Clinical Trial Registration Number:
NCT04788823.
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