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N/A Completed N=11 Supportive Care

Lorazepam, Diphenhydramine Hydrochloride, and Haloperidol Gel in Healthy Volunteers

Healthy
Source: ClinicalTrials.gov NCT01204255 ↗
Enrolled (actual)
11
Serious AEs
0.0%
Results posted
Aug 2011
Primary outcomePrimary: Lorazepam, Diphenyhydramine, Haloperidol Absorption — 0; .08; 0 ng/ml

Summary

RATIONALE: Lorazepam, diphenhydramine hydrochloride, and haloperidol gel, when absorbed into the skin, may be an effective treatment for nausea and vomiting.PURPOSE: This clinical trial studies lorazepam, diphenhydramine hydrochloride, and haloperidol gel in healthy volunteers.

Outcome Measures

OutcomeResultp-value
PRIMARY
Lorazepam, Diphenyhydramine, Haloperidol Absorption
0; .08; 0
SECONDARY
Side Effects

Eligibility Criteria

Inclusion Criteria

  • Completed a medical screening questionnaire
  • English speaking
  • No allergies to the drugs
  • Able to complete the forms
  • If a woman of childbearing age, agree to use contraception

Exclusion Criteria

  • History of substance abuse, psychiatric disorder, acquired brain injury, the possibility of pregnancy (not using birth control, and of child bearing age)
  • Use of any medication that would contraindicate benzodiazepine administration
  • Pregnant or nursing
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01204255). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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