Overview

Precise Use of Lidocaine Cream to Treat Primary Premature Ejaculation

Status:
Recruiting
Trial end date:
2023-04-01
Target enrollment:
0
Participant gender:
Male
Summary
This study aimed to evaluate the efficacy and safety of applying 5% lidocaine cream to the sensitive area of the glans penis after its precise localization under the penile biological vibration threshold test for the treatment of primary premature ejaculation.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Second Affiliated Hospital, School of Medicine, Zhejiang University
Treatments:
Lidocaine
Criteria
Inclusion Criteria:

- adult male (19-60 years old); stable partner for ≥3 months; Premature Ejaculation
Diagnostic Tool (PEDT) score ≥ 11; penile biological vibration threshold test
suggesting the presence of sensitive sites on the glans penis (vibration threshold <
30 levels); no history of long-term use of specific medications; normal sex hormone
levels; and no genital or secondary ejaculation. There was no history of long-term use
of specific drugs, normal sex hormone levels, and genital or secondary sexual
characteristics abnormalities.

Exclusion Criteria:

- (1) those with abnormal or malformed genital development; (2) those with allergic
reactions to local anesthetics; (3) those who had been treated with central nervous
system drugs or PE in the last 3 months; (4) those with a history of long-term alcohol
abuse and trauma such as neurological and pelvic fractures; (5) those with long-term
use of hypotensive drugs, diuretics, and sedative drugs (6) patients with a history of
previous surgery and trauma to the reproductive system; (7) patients with PE due to
hypogonadism, thyroid disease, and abnormal lipid metabolism.