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, Daniela Orozco Rendon, BS Baylor College of Medicine , The Scott Department of Urology, Houston, TX , United States Search for other works by this author on: Oxford Academic Gal Saffati, MD Baylor College of Medicine , The Scott Department of Urology, Houston, TX , United States Search for other works by this author on: Oxford Academic Christine Whitehead, BSN, RN Reproductive Medicine Associates of New Jersey , Basking Ridge, NJ , United States Search for other works by this author on: Oxford Academic Caroline Zuckerman, BS, RN Reproductive Medicine Associates of New Jersey , Basking Ridge, NJ , United States Search for other works by this author on: Oxford Academic Amy Hom, BS Reproductive Medicine Associates of New Jersey , Basking Ridge, NJ , United States Search for other works by this author on: Oxford Academic Riley Daily, MS FirmTech, Inc. , Bozeman, MT , United States Search for other works by this author on: Oxford Academic Mohit Khera, MD, MPH, MBA Baylor College of Medicine , The Scott Department of Urology, Houston, TX , United States Search for other works by this author on: Oxford Academic Philip J Cheng, MD Reproductive Medicine Associates of New Jersey , Basking Ridge, NJ , United States Corresponding author: Department of Urology, Reproductive Medicine Associates of New Jersey, NJ 07920, United States. Email: philipj.cheng@gmail.com Search for other works by this author on: Oxford Academic
The Journal of Sexual Medicine, qdae151, https://doi.org/10.1093/jsxmed/qdae151
Published:
14 November 2024
Article history
Received:
17 April 2024
Revision received:
07 October 2024
Accepted:
23 October 2024
Published:
14 November 2024
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Daniela Orozco Rendon, Gal Saffati, Christine Whitehead, Caroline Zuckerman, Amy Hom, Riley Daily, Mohit Khera, Philip J Cheng, Penile constriction devices: a randomized survey study to compare preferences between two medical-grade devices, The Journal of Sexual Medicine, 2024;, qdae151, https://doi.org/10.1093/jsxmed/qdae151
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Abstract
Background
Penile constriction devices offer a noninvasive approach to enhance the sexual experience and as the variety of penile constriction devices increases, it is crucial to assess patient preferences and device effectiveness to provide insights into their clinical utility.
Aim
We aimed to compare the preferences for and effectiveness of two medical-grade penile constriction devices: Eddie by Giddy and FirmTech.
Methods
Between May and July of 2023, males were recruited via social media and prospectively enrolled into an Institutional Review Board-approved, randomized, questionnaire-based study. Upon enrollment, the participants completed the Sexual Health Inventory for Men and Androgen Deficiency in Aging Males questionnaires. Participants were randomized to which device they received first. They used the device twice either during masturbation or intercourse in a two-week timeframe. Once utilized, the participants completed a 17-question, Likert scale, device satisfaction questionnaire, in which lower numbers indicated positive responses. The process was repeated with the second device. T-test and Chi-Square Analysis were run for statistical analysis.
Outcomes
The primary outcomes of this study were patient-reported device satisfaction and efficacy and the secondary outcome was the device preference for patients with and without erectile dysfunction.
Results
Fifty men were enrolled and 49 completed the study. The average age was 40years old. Of the participants, 80% recommend the FirmTech device compared to 53% who recommend the Eddie by Giddy device (P= 0.0026). The FirmTech device was overall easier to put on both flaccid and erect (P= 0.0308 and 0.0002), was more comfortable, had better stretch, and was easier to adjust (P= 0.087, <0.0001, and 0.0119, respectively). The FirmTech device had a better overall impression amongst the participants (P= 0.0249). Eddie by Giddy was felt to improve erectile firmness more in those with ED than in those without (P = 0.0178).
Clinical Implications
This study adds to the current literature on penile constriction devices that better guide providers as they counsel patients on these devices to enhance sexual function.
Strengths and Limitations
The strength of this study is that this is a prospective randomized crossover study. The limitations of this study are that this is a single center study based on patient reported outcomes.
Conclusion
The FirmTech device performed better than the Eddie by Giddy with respect to overall impression of the device, likelihood of using the device in the future, and recommending the device to a friend, while the Eddie by Giddy device performed better at improving erectile firmness.
Clinical Trial Registration Number
NCT05853822.
erectile dysfunction, sex tools, penile constriction device, patient satisfaction
© The Author(s) 2024. Published by Oxford University Press on behalf of The International Society for Sexual Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/pages/standard-publication-reuse-rights)
Issue Section:
Erectile Function
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