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NCT00483990 · ClinicalTrials.gov registry record · Phase 1

Phase I Study of PSD502 (Lidocaine Prilocaine Spray) Applied to the Glans Penis up to Three Times a Day for 21 Days in Healthy Male Volunteers

A Phase 1 study of Healthy, sponsored by Plethora Solutions.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target
1
Study location

NCT00483990: Completed Phase 1 study of Healthy, sponsored by Plethora Solutions.

NCT00483990 is a Phase 1 study of Healthy that has completed, run by Plethora Solutions. The registered enrollment target is 16 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00483990, a Phase 1 study of Healthy, has completed, sponsored by Plethora Solutions.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target
1
Study location

Study Summary

The main objective of the study is to determine the safety and tolerability of repeated application of PSD502 to the glans penis in healthy male volunteers

Conditions Studied

Interventions

  • DRUG PSD502

Study Locations (1)

Kansas

  • PRA International - Clinical Pharmacology Center - Lenexa

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2007-03
Est. Completion 2007-06
Phase Phase 1
Plethora Solutions

3 total trials

What the finished NCT00483990 record still lists

NCT00483990 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 1 intervention - of which PSD502 is the first listed.

NCT00483990 reports a single indexed study location in Kansas.

Frequently Asked Questions

What is clinical trial NCT00483990 about?

NCT00483990 is a clinical study titled "Phase I Study of PSD502 (Lidocaine Prilocaine Spray) Applied to the Glans Penis up to Three Times a Day for 21 Days in Healthy Male Volunteers". The main objective of the study is to determine the safety and tolerability of repeated application of PSD502 to the glans penis in healthy male volunteers

What is the current status of trial NCT00483990?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2007-03. Estimated completion is 2007-06.

What conditions does trial NCT00483990 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT00483990?

The interventions under investigation include: PSD502 (DRUG).

Who is sponsoring clinical trial NCT00483990?

This trial is sponsored by Plethora Solutions, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00483990 being conducted?

This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00483990's enrollment target sits among peer trials

16 936th of 1090 higher than 137 of 1,090 other Healthy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00483990, the US trial registry maintained by the National Library of Medicine. NCT00483990 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.