The Effects of Antihistamines on Pre-Pulse Inhibition (PPI)

This study has been completed.
Sponsor:
Collaborator:
Wallace Foundation
Information provided by (Responsible Party):
Duke University
ClinicalTrials.gov Identifier:
NCT01537471
First received: February 1, 2012
Last updated: January 15, 2013
Last verified: January 2013
  Purpose

The purpose of the investigators research is to test whether problems people have with processing their senses (feeling overwhelmed, distracted or upset by sounds and other stimuli) can be lessened by meclizine, a drug found in many over the counter antihistamines, which are medicines used for things like allergies, sleep problems, or the common cold.


Condition Intervention Phase
Healthy
Drug: Placebo
Drug: Meclizine
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: A Pilot Study of the Effects of Meclizine on Pre-Pulse Inhibition

Resource links provided by NLM:


Further study details as provided by Duke University:

Primary Outcome Measures:
  • Change in PPI [ Time Frame: Screening Day 1, Days 2-4 ] [ Designated as safety issue: No ]
    The primary outcome will measure change in subjects' PPI depending on whether they were given meclizine during the study. Prepulse inhibition (PPI) of the startle reflex by a weak pre-pulse will be assessed during each laboratory session. It is measured using electromyographic (EMG; i.e., for assessing eye blink magnitude) responses.


Secondary Outcome Measures:
  • Sedation [ Time Frame: Day 2, Day 3, & Day 4 ] [ Designated as safety issue: Yes ]
    A Baseline sedation level at the beginning of each visit will be collected. Then study drug (meclizine/placebo) will be given and a sedation level will be collected at 20 minutes and 40 minutes post drug as well as during the PPI experiment pre & post. The Sedation scale will be used (a modified version of the SAM scale).


Enrollment: 117
Study Start Date: January 2012
Study Completion Date: September 2012
Primary Completion Date: September 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Placebo
A counterbalanced design will be used with each male subject receiving placebo and each of the anti-histamine low (12.5 mg) and high (25 mg) doses in a counterbalanced order to keep order of administration from being confounded with dose level. On one of three visits, a subject will receive placebo. The subject, study coordinator, co-investigator and outcomes assessor will remain blinded to what they received until data analysis is completed.
Drug: Placebo
Placebo
Other Name: Sugar Pill
Experimental: Meclizine
A counterbalanced design will be used with each male subject receiving placebo and each of the anti-histamine low (12.5 mg) and high (25 mg) doses in a counterbalanced order to keep order of administration from being confounded with dose level. By the time they finish, they will have all received placebo, 12.5mg meclizine and 25mg meclizine. The subject, study coordinator, co-investigator and outcomes assessor will remain blinded to what they received until data analysis is completed.
Drug: Meclizine
Meclizine 12.5 mg
Other Name: Antivert, Dramamine II, Bonine, Medivert
Drug: Meclizine
Meclizine 25 mg
Other Name: Antivert, Dramamine II, Bonine, Medivert

  Hide Detailed Description

Detailed Description:

This experiment will test the efficacy of acute anti-histamine doses on the acoustic startle response and prepulse inhibition (or PPI, a well-known neurobehavioral phenomenon used to characterize sensorimotor modulation described in detail below) in a male population with high baseline sensory startle levels. In addition, sex differences in baseline PPI (i.e. without anti-histamine administration) in subjects of this population will be investigated.

The main hypothesis of the study is that the H1¬-antagonist meclizine will be effective in restoring low levels of PPI observed in the subject pool so that sensory gating is made more effective. The dependent measures will be startle response magnitude and pre-pulse inhibition.

The experiment will take place in four sessions, carried out on different days. Consecutive test sessions will take place no earlier than 3 days, and no longer than 21 days apart. Before being recruited into the study, potential participants will go through a phone screen-a pre-experiment screening questionnaire (separate) to exclude subjects with neurological disorders, certain psychiatric disorders, who smoke or use nicotine products, or who use certain drugs (see exclusion criteria below) as they can affect PPI levels. If they are eligible per the phone screen, subjects will come in for screening (test day 1). They will be again asked about their tobacco/nicotine use and what medications they are currently taking. They will be asked about their caffeine history use. Caffeine and caffeine withdrawal both have effects on startle response but not on PPI so we are not restricting subject's caffeine use, but collecting this information. CO levels will be collected using a CO monitor to confirm that participants have not recently used a tobacco product. They will be asked questions about psychiatric symptoms, personality, and how they cope with stress. Participants' startle responses and PPI will be tested in the laboratory (see below).

During the following three test days (2-4) before dispensing study drug, male participants who qualify, will be asked to fill out a questionnaire about tobacco or nicotine use since their previous visit along with assessing any change in their medications (specifically verifying that a male participant has not used an allergy, cold/flu medication within 3 days of their study visit). If the participant answers yes to either question, they will be asked to return to the clinic on a different day: 1) 3 or more days post using an antihistamine or 2) at least 2 weeks post using tobacco or nicotine. Both antihistamine medications or tobacco/nicotine recent use can effect a participant's PPI which is why we have the need to ask male participants about any possible changes. They will also be asked how they arrived to the clinic to verify that they have a driver who came with them/dropped them off, had a hired driver provided by the study if they live in Durham or came by bus or by foot. They will be asked about their caffeine use on the day of their experiment. Their baseline sedation level will be assessed. On test days 2-4, the test procedure employed on test day 1 will be repeated, but 60 minutes before the start of each test sessions, participants will receive a placebo, a low (12.5 mg) dose of meclizine, or a high (25 mg) dose of this drug in a counterbalanced order.

Male participants (n = 20) will receive the study medication or placebo orally and will be provided water at administration at visits Day 2-4. Placebo and meclizine capsules will be identical in shape, size, and color. The randomization and counterbalancing of the order of dosing will be in charge of Dr. Levin. In order to ensure that the blind procedure is not violated, Dr. Levin (a) will provide the identical capsules for the study to the Study Coordinator in containers labeled "Subject X, day Y", and (b) will have no contact with the participants in the study. Meclizine and placebo will be dispensed by the Study Coordinator under the administrative supervision of Dr. Rosenthal, and under the clinical supervision of a study physician. During the resting period between pill ingestion and the experimental task, male participants will be asked to sit in a lab room and read or use the internet. At 20 minutes and 40 minutes post drug, sedation level will be assessed using the scale listed below.

In each PPI test session throughout all 4 visits, male participants will begin with a resting baseline period of 5 minutes, where they will be asked to sit quietly and still in a sound and temperature controlled lab room, with their eyes open looking at a fixation cross on the monitor. Baseline is conducted to obtain measures of emotional arousal and sedation prior to the experimental manipulations. As such, during baseline psychophysiological measures will be collected. Self-reported emotional arousal will be obtained at the beginning and end of the baseline period using the Self-Assessment Manikin (Bradley, 1999), which assesses arousal and valence of affective state using Likert (1-9) scales. Self-reported level of sedation will be assessed at the same time points as emotional arousal (using a modified Self-Assessment Manikin using the same Likert 1-9 scale). Next, participants will be exposed to an initial adaptation phase, in order for them to become acquainted with the startle stimuli (pulses and prepulses), and their startle responses reach a stable level. In this phase, 4 blocks of prepulse-pulse (pP) and pulse-alone (P) trials will be presented, with an inter-trial interval (ITI) of 20 seconds (+/- 5 sec). After the initial adaptation phase, participants will be instructed to view a computer monitor where random geometric figures will be presented, while simultaneously 10 blocks of auditory pP and P trials will be presented with an ITI of 20 sec. Each test session will last around 15 minutes. At the end of the test session, the standardized lab test to assess the participants' attention level described above will be presented again.

Females will only complete the first day of testing (in the same way as described for male subjects above).

  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 18-40 males or females
  • Startle response >0.5
  • PPI < 32
  • CO level <8ppm

Exclusion Criteria:

  • Tobacco or nicotine use within 2 weeks of screening
  • Current or history of a neurological disorder of neurological event
  • Negative response to antihistamine use in past
  • ECT treatment in the past 6 months
  • Current or past history of manic or hypomanic episodes (SCID-I)
  • Current or history of psychotic disorder
  • Current alcohol or substance abuse/dependence
  • Positive urine drug test
  • CO level of >8ppm
  • Startle <0.5 & overall PPI >32 (assessed during study)
  • Significant hearing problem
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01537471

Locations
United States, North Carolina
Duke University Medical Center
Durham, North Carolina, United States, 27705
Sponsors and Collaborators
Duke University
Wallace Foundation
Investigators
Principal Investigator: Mark Z Rosenthal, PhD Duke University
Principal Investigator: Ed Levin, MD Duke University
  More Information

Publications:
Responsible Party: Duke University
ClinicalTrials.gov Identifier: NCT01537471     History of Changes
Other Study ID Numbers: Pro00028299
Study First Received: February 1, 2012
Last Updated: January 15, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by Duke University:
PPI
Meclizine
Startle
Sensory processing
antihistamines

Additional relevant MeSH terms:
Histamine Antagonists
Meclizine
Dimenhydrinate
Histamine H1 Antagonists
Histamine Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Physiological Effects of Drugs
Antiemetics
Autonomic Agents
Peripheral Nervous System Agents
Central Nervous System Agents
Therapeutic Uses
Gastrointestinal Agents
Anti-Allergic Agents

ClinicalTrials.gov processed this record on August 26, 2014