Clinical outcomes of selective dorsal cryoneurolysis in patients with lifelong premature ejaculation: a retrospective cohort of 108 men
In brief
Selective dorsal cryoneurolysis quadruples ejaculatory latency to about four minutes
In a retrospective series of 108 men with lifelong premature ejaculation, median intravaginal ejaculatory latency time rose from 54 seconds to 231 seconds and stayed elevated through 12 months, while patient-reported scores improved and no erectile dysfunction occurred. About one in ten men did not achieve a meaningful response, and the procedure's long-term comparative efficacy remains unproven.
- Journal
- The journal of sexual medicine (Q1)
- Published
- 14 September 2026
- Study design
- Randomized controlled trial
- Evidence level
- Level 1, High (CEBM 1b)
- Authors
- Yasar Basaga, Ahmet Tevfik Albayrak, Zulfu Sertkaya, Ege Can Serefoğlu
- PMID
- 42747863
- DOI
- 10.1093/jsxmed/qdag284
Why clinicians should know about it
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Abstract
BACKGROUND: Selective dorsal cryoneurolysis (SDC) is a minimally invasive, potentially reversible neuromodulatory intervention for men with lifelong premature ejaculation (PE) refractory to conventional therapy. AIM: To evaluate the efficacy, safety, and objective sensory effects of SDC in men with lifelongPE. METHODS: This retrospective cohort included 108 men with lifelong PE (mean age 40.4 ± 11.6 years; body mass index 25.5 ± 3.2 kg/m2) who underwent SDC between January 2024 and January 2025. All reported stopwatch-measured intravaginal ejaculatory latency time (IELT) <1 min, normal erectile function, and inadequate response to pharmacological and behavioral treatment. Intravaginal ejaculatory latency time, Premature Ejaculation Diagnostic Tool (PEDT), Premature Ejaculation Profile (PEP), penile vibration-perception thresholds (biothesiometry), adverse events, and treatment failure were assessed to 12 months. Complete data were available for all patients, with no loss to follow-up. Normality was tested with Shapiro-Wilk; changes over time were analyzed with Wilcoxon signed-rank and paired t-tests and the Friedmantest. OUTCOMES: The primary outcome was change in IELT; secondary outcomes were PEDT and PEP scores and adverse events. RESULTS: Geometric-mean IELT rose from 54.4 s (95% confidence interval [CI], 45.8-64.5) to 231.3 s at 12 months (95% CI, 209.1-256.0)-an approximately 4-fold improvement first reached by month 3 and sustained thereafter (P < .001). Premature Ejaculation Diagnostic Tool decreased from 14.3 ± 2.3 to 8.4 ± 2.1 and the total PEP score increased from 6.0 ± 2.0 to 11.6 ± 2.4 (both P < .001). Penile thresholds rose from ~4.5 to ~10.7 V at all sites (P < .001), confirming objective desensitization. Procedure-related discomfort occurred in 8/108 patients (7.4%), all mild and self-limiting, and persistent PE in 11/108 (10.2%); 82/108 (75.9%) underwent a second and 22/108 (20.4%) a third session. No erectile dysfunction, anorgasmia, persistent numbness, or infection occurred. CLINICAL IMPLICATIONS: Selective dorsal cryoneurolysis provides significant, sustained improvements in ejaculatory latency and patient-reported outcomes without compromising sexual function, although approximately one in ten patients did not achieve a meaningful response. STRENGTHS AND LIMITATIONS: Strengths include a relatively large cohort, standardized outcome measures, and objective sensory (biothesiometry) testing. Limitations include the retrospective, uncontrolled, non-randomized design, and the absence of partner-reported outcomes. CONCLUSION: Selective dorsal cryoneurolysis appears to be a safe, effective, minimally invasive, and potentially reversible option for refractory lifelong PE, positioned between pharmacotherapy and permanent neurotomy. It remains investigational, and prospective randomized controlled trials are warranted to confirm long-term durability and comparative efficacy.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.