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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03459833
Other study ID # PE:HA glans augmentation
Secondary ID
Status Completed
Phase Phase 3
First received February 12, 2018
Last updated March 10, 2018
Start date August 19, 2016
Est. completion date March 2018

Study information

Verified date March 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized controlled cross-over study aims to evaluate the effect and safety of glans penis augmentation using Hyaluronic acid in the treatment of premature ejaculation in compare with placebo .


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender Male
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- occurrence of ejaculation in patients with lifelong premature ejaculation (LL PE) within 1 minute form vaginal penetration in all or almost all occasions starting from the first sexual experience, and within 3 minutes in patients with acquired premature ejaculation (A PE), along with inability to delay ejaculation on all or nearly all vaginal penetrations, with negative personal consequences, such as distress, bother, frustration, and/or the avoidance of sexual intimacy

Exclusion Criteria:

- Erectile dysfunction

- Hypo or hyperthyroidism

- Hypogonadism

- Hyperprolactinemia

- Drug abuse

- Psychiatric disorders or related medications

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Hyaluronic Acid
Glans penis augmentation using multiple puncture technique as described by Abdallah et al. (2012) with minor modifications. HA is injected at two circular levels: one at the level of corona of glans penis and a second circular level is mid-way between the corona and urethral meatus. Six injections are injected at coronal level and four are injected in the second level, each injection is of 0.2 ml and is injected into deep dermis.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary IELT Intra-vaginal Ejaculation Latency Time Change from baseline after one month
Primary AIPE Arabic index of premature ejaculation Change from baseline after one month
Secondary IELT Intra-vaginal Ejaculation Latency Time Change from baseline after three, six and nine months
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