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Trial · NCT02155309

Pharmacokinetic and Efficacy Profile Intranasal Scopolamine Spray

NCT02155309, Phase 2, Phase 3, Terminated, Repurposed Therapeutics, Inc.; results first posted 2018-01-17

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pharmacokinetic and Efficacy Profile Intranasal Scopolamine Spray. Trials, record NCT02155309. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02155309

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Pharmacokinetic and Efficacy Profile Intranasal Scopolamine Spray
NCT number
NCT02155309
Status
Terminated
Phases
Phase 2, Phase 3
Enrollment
63 participants, actual
Lead sponsor
Repurposed Therapeutics, Inc.
Conditions
Motion Sickness
Interventions
Scopolamine, Placebo
First posted
2014-06-04
Last updated
2018-01-17
Results first posted
2018-01-17

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryEfficacy: Number of Head Movements During Rotation40 min
During rotation, efficacy is measured by the number of head movements subjects are able to make (12 per minute). While seated yaw-axis rotating, a pre-recorded computerized voice informed subjects to make paced head tilts of 30 ̊ to the right and left at a rate of 0.125 Hz (right, center, left, and back to center over 16 seconds).

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYEfficacy: Number of Head Movements During Rotation40 minNumber of head tiltsMEAN

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Efficacy: Number of Head Movements During RotationEfficacy: Scopolamine and Placebo (Crossover, Double-blind)Head Tilts: Scopolamine Condition222.5Standard Deviation 105Number of head tilts
Efficacy: Number of Head Movements During RotationEfficacy: Scopolamine and Placebo (Crossover, Double-blind)Head Tilts: Placebo Condition191.7Standard Deviation 95.1Number of head tilts

Participant flow9

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPK: Scopolamine Only, Open-label13
Overall StudySTARTEDEfficacy: Scopolamine, Then Placebo10
Overall StudySTARTEDEfficacy: Placebo, Then Scopolamine13
Overall StudyCOMPLETEDPK: Scopolamine Only, Open-label13
Overall StudyCOMPLETEDEfficacy: Scopolamine, Then Placebo10
Overall StudyCOMPLETEDEfficacy: Placebo, Then Scopolamine12
Overall StudyNOT COMPLETEDPK: Scopolamine Only, Open-label0
Overall StudyNOT COMPLETEDEfficacy: Scopolamine, Then Placebo0
Overall StudyNOT COMPLETEDEfficacy: Placebo, Then Scopolamine1

Adverse events3

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherNonserious AEsGeneral disordersPK: Scopolamine Only, Open-label111342
otherNonserious AEsGeneral disordersEfficacy: Scopolamine (Crossover, Double-blind)182382
otherNonserious AEsGeneral disordersEfficacy: Placebo (Crossover, Double-blind)192365

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPK: Scopolamine Only, Open-label013
Total, all-cause mortalityEfficacy: Scopolamine (Crossover, Double-blind)023
Total, all-cause mortalityEfficacy: Placebo (Crossover, Double-blind)023
Total, other adverse eventsPK: Scopolamine Only, Open-label1113
Total, other adverse eventsEfficacy: Scopolamine (Crossover, Double-blind)1823
Total, other adverse eventsEfficacy: Placebo (Crossover, Double-blind)1923
Total, serious adverse eventsPK: Scopolamine Only, Open-label013
Total, serious adverse eventsEfficacy: Scopolamine (Crossover, Double-blind)023
Total, serious adverse eventsEfficacy: Placebo (Crossover, Double-blind)023

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
11297908BACKGROUND

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02155309

GET https://conductscience.org/api/trials/v1/NCT02155309/registered