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. 2019 May 25;2019(5):CD012832. doi: 10.1002/14651858.CD012832.pub2

1. Baseline characteristics of included studies.

Study name Trial
 period
 (year to
 year) Setting/country Description of participants Intervention(s)
and
comparator(s)
Duration of follow‐up Age (mean ± SD) IPSS
(mean ± SD)
Prostate volume
(mean ± SD)
Gratzke 2017 February 2012 to October 2013 10 centres/Europe Men aged ≥ 50 years with IPSS > 12, Qmax ≤ 15 mL/second for 125 mL voided volume, postvoid residual volume < 350 mL, prostate volume ≤ 60 mL on ultrasound, sexually active within 6 months before the index procedure, Sexual Health Inventory for Men score > 6, positive response to MSHQ‐EjD (excluding the response "Could not ejaculate"), Incontinence Severity Index score ≤ 4 PUL 24 months 63 ± 6.8 years 22 ± 5.7 38 ± 12 mL
TURP 65 ± 6.4 years 23 ± 5.9 41 ± 13 mL
Roehrborn 2013 February to December 2011 19 centres/US, Canada, and Australia Men ≥ 50 years old, provided informed consent, had no prior surgical treatment for BPH, and were required to undergo washouts of 2 weeks for alpha‐blocker, 3 months for 5a‐reductase inhibitor, and 3 days for anticoagulants. Admission to the study required AUASI ≥ 13, Qmax ≤ 12 mL/second with a 125 mL voided volume and a 30–80 mL prostate volume PUL 3 months 67 ± 8.6 year 22.2 ± 5.48 44.5 ± 12.4 mL
Sham 65 ± 8.0 years 24.4 ± 5.75 40.9 ± 10.8 mL

AUASI: American Urological Association Symptom Index; BPH: benign prostatic hyperplasia; IPSS: International Prostate Symptom Score; MSHQ‐EjD: Male Sexual Health Questionnaire for Ejaculatory Dysfunction; PUL: prostatic urethral lift; Qmax: maximum flow rate; TURP: transurethral resection of prostate.