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Clinical Trial Summary

Introducing and evaluating the accuracy of a novel method for estimating inflatable penile prosthesis cylinders length by stretching the tumesncent penis intraoperatively instead of taking proximla and distal measurement to the corporotomy


Clinical Trial Description

Objectives: Introducing and evaluating the accuracy of a novel method for estimating inflatable penile prosthesis cylinders length. Methods: 24 patients undergoing a Coloplast Titan ® Touch implantation procedure will berandomly divided into two groups. The "Tumescent Stretching Measurement Technique" (TSMT) group (N=12) will be administered an intracorporal injection (ICI) of 20 microgram Alprostadil. Hegar 7 dilator will be introduced through the corporotomy until reaching a bone stopping point. The tumescent penis will be stretched maximally, and the proximally inserted dilator measured externally to the coronal sulcus. The control group (N=12) will receive no intraoperative ICI. Following maximal corporal dilatation, cylinder length will be estimated by adding up the internally measured distal and proximal corpora to the length of the corporotomy. Implants are deemed correctly sized when cylinders reached the proximal third of the glans with no buckling of cylinders or floppy glans. ;


Study Design


NCT number NCT04864301
Study type Interventional
Source Cairo University
Contact
Status Active, not recruiting
Phase N/A
Start date January 1, 2019
Completion date May 1, 2021