Medical test

Medical test with a penis traction device

This case study shows how penis traction can enlarge penis size. The patients in this study are between 23-47 years old and they all showed permanent results and no complications! The average lengthening per week was 1.2 mm.

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1. In troduction

Based on the evidence of human tissue response to stretching, a traction device for non-invasive penile lengthening has been designed and tested.

Traction device

– Basic ring, fastened proximally around the root of the penis, abutting on the symphysis.
– Two adjustable metal bars hinged to the ring, connecting it to the silicon-support, fastened around the corona glandis at the distal end of the penis.
– By gradually increasing the tractive force on the two metal bars a stretching force is exerted on the corporae, which equals a tractive force of a 600-1500 g weight attached to the penis.

2. Material andmethods

Number of Patients: 10 Patients raging from 23-47 years.
Patient Selection

Inclusion: Normal erectile capacity and no penile surgery

Exclusion: Chronically diseases

Traction Force

0 - 2 weeks: 900 - 1000g

2 - 26 weeks: 1000 - 1200g

Treatment Period12 hours daily 7 days a week 8 to 26 weeks
Follow UpEvery 2 weeks

3. Results and results in erection

Weeks Length Before Length After Difference Length (%)
Mean (cm)
14,8
12
15,3
3,3
28
Range (cm)
(8-24)
(9,5 - 15,0)
(15,5 - 18,5)
(1,5 - 5,0)
(10 - 42)

4. Conclusions

Preliminary study

– All patients achieved penile lengthening after traction

– Lengthening per week was 1,2 mm

– No complications

– Medical indications:

a) non-invasive: hypoplasic penis, Peyronie’s

b) postoperative: hypospadias / epispadias, penile lengthening procedures

1st International Interdisciplinary Symposium on Genitourinary Reconstructive Surgery in Congenital Malformations, Transsexuals, and Impotence Barcelona, Spain, April 6, 7, and 8, 1998

http://onlinelibrary.wiley.com/doi/10.1002/j.1939-4640.1998.tb02485.x/abstract

MaleEdge products are certified medical devices with safety and efficacy assessed under Medical Device Directive 93/42/EEC in Europe.

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