Skip to main content
OpenTrials
Completed

NCT Number: NCT02578186

Evaluation of Diphenhydramine Hydrochloride Effects in Subjects With Occasional Sleeplessness

The present study was conducted to investigate the impact of diphenhydramine hydrochloride on the ability to initiate sleep.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

About this study

Diphenhydramine hydrochloride (herein referred to as diphenhydramine) is an antihistamine of the ethanolamine classes with known sleep-inducing properties and is approved by the Food & Drug Administration to reduce the time to sleep onset in individuals having difficulty falling asleep. The goal of the study is to investigate diphenhydramine versus placebo with regard to several sleep parameters, including time to sleep onset, in healthy adult subjects suffering from occasional sleeplessness.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • be male or female subjects, ≥18 years of age to 55 years of age, who report that they are currently experiencing occasional sleeplessness characterized by difficulty initiating sleep (ie, taking ≥30 minutes to fall asleep) on average 2-4 times per week for less than 1 month;
  • be in good general health without clinically significant disease (no previously diagnosed sleep disorders);
  • if female, have a negative screening pregnancy test and agree to be on approved methods of birth control throughout the study

Exclusion criteria

  • have a clinically significant illness within 30 days of Screening;
  • are taking medication that could interfere with the study medication;
  • have been under a clinician's care for insomnia treatment and control within the past year or has a history of insomnia or is currently taking prescription medications for insomnia;
  • are currently taking medications known to effect sleep function;
  • have current or past history of serious, severe or unstable physical or psychiatric illness;
  • have current diagnosis of severe urinary retention;
  • have current diagnosis of untreated narrow angle glaucoma;
  • had participated in a clinical drug study or used an investigational new drug during the previous 30 days;
  • have any clinically significant or abnormal finding in physical examination, vital signs, ECG, or clinical laboratory tests that may affect the subject's safety or outcome of the study;

Treatment and study plan

Diphenhydramine hydrochloride

Drug

30 mL at bedtime

Other names: Zzzquil

Placebo

Drug

30 mL at bedtime

Other names: placebo comparator

Primary outcomes

  1. Mean Latency to Persistent Sleep

    Time frame: 4 weeks

    Per Protocol population based on subjects who completed treatment crossover

Sponsors and collaborators

Lead sponsor

Procter and Gamble

Industry

Registry information

Official study title

Randomized, Double-Blind, Placebo-Controlled, Crossover, In-home Study to Assess the Efficacy of Diphenhydramine Hydrochloride in Subjects With Occasional Sleeplessness

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Oct 16, 2015
Registry last updated
Mar 15, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.