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Trial · NCT02307526

Acetylcholinesterase Inhibition and Orthostatic Hypotension in SCI

NCT02307526, Phase 2, Completed, James J. Peters Veterans Affairs Medical Center; results first posted 2017-07-21

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Acetylcholinesterase Inhibition and Orthostatic Hypotension in SCI. Trials, record NCT02307526. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02307526

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Trial

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

Title
Acetylcholinesterase Inhibition and Orthostatic Hypotension in SCI
NCT number
NCT02307526
Status
Completed
Phases
Phase 2
Enrollment
10 participants, actual
Lead sponsor
James J. Peters Veterans Affairs Medical Center
Conditions
Hypotension, Postural
Interventions
Pyridostigmine Bromide, Tilt table test
First posted
2014-12-04
Last updated
2017-07-21
Results first posted
2017-07-21

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimarySystolic Blood Pressure
Average systolic blood pressure of 10 minutes supine rest before pyridostigmine and after 45 minutes at 45 degrees after pyridostigmine administration compared to 10 minutes supine rest before tilt and at 45 degrees during no-drug head-up tilt maneuver.
PrimaryDiastolic Blood Pressure
Average diastolic blood pressure of 10 minutes supine rest before pyridostigmine and after 45 minutes at 45 degrees after pyridostigmine administration compared to 10 minutes supine rest before tilt and at 45 degrees during no-drug head-up tilt maneuver.
PrimaryHeart Rate
Average heart rate of 10 minutes supine rest before pyridostigmine and after 45 minutes at 45 degrees following pyridostigmine administration compared to 10 minutes supine rest before tilt and at 45 degrees during no-drug head-up tilt maneuver.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYSystolic Blood Pressure
Average systolic blood pressure of 10 minutes supine rest before pyridostigmine and after 45 minutes at 45 degrees after pyridostigmine administration compared to 10 minutes supine rest before tilt and at 45 degrees during no-drug head-up tilt maneuver.
mm HgMEAN
PRIMARYDiastolic Blood Pressure
Average diastolic blood pressure of 10 minutes supine rest before pyridostigmine and after 45 minutes at 45 degrees after pyridostigmine administration compared to 10 minutes supine rest before tilt and at 45 degrees during no-drug head-up tilt maneuver.
mm HgMEAN
PRIMARYHeart Rate
Average heart rate of 10 minutes supine rest before pyridostigmine and after 45 minutes at 45 degrees following pyridostigmine administration compared to 10 minutes supine rest before tilt and at 45 degrees during no-drug head-up tilt maneuver.
bpmMEAN

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Systolic Blood PressurePyridostigmine BromideSupine Systolic Blood Pressure97Standard Deviation 11mm Hg
Systolic Blood PressureNO DrugSupine Systolic Blood Pressure103Standard Deviation 14mm Hg
Systolic Blood PressurePyridostigmine Bromide45 degree Head-up Tilt Systolic Blood Pressure90Standard Deviation 18mm Hg
Systolic Blood PressureNO Drug45 degree Head-up Tilt Systolic Blood Pressure88Standard Deviation 12mm Hg
Diastolic Blood PressurePyridostigmine BromideSupine Diastolic Blood Pressure64Standard Deviation 6mm Hg
Diastolic Blood PressureNO DrugSupine Diastolic Blood Pressure66Standard Deviation 10mm Hg
Diastolic Blood PressurePyridostigmine Bromide45 degree Head-up Tilt Diastolic Blood Pressure64Standard Deviation 11mm Hg
Diastolic Blood PressureNO Drug45 degree Head-up Tilt Diastolic Blood Pressure63Standard Deviation 7mm Hg
Heart RatePyridostigmine BromideSupine Heart Rate52Standard Deviation 6bpm
Heart RateNO DrugSupine Heart Rate55Standard Deviation 10bpm

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Day 1 - No DrugSTARTEDSpinal Cord Injury10
Day 1 - No DrugCOMPLETEDSpinal Cord Injury10
Day 1 - No DrugNOT COMPLETEDSpinal Cord Injury0
Day 2 - 60 mg of PyridostigmineSTARTEDSpinal Cord Injury10
Day 2 - 60 mg of PyridostigmineCOMPLETEDSpinal Cord Injury10
Day 2 - 60 mg of PyridostigmineNOT COMPLETEDSpinal Cord Injury0

Adverse events4

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

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousDrug Side EffectNervous system disordersDay 1 - No Drug0100
seriousDrug Side EffectNervous system disordersDay 2 - Pyridostigmine Bromide1101
seriousOverheatingNervous system disordersDay 1 - No Drug0100
seriousOverheatingNervous system disordersDay 2 - Pyridostigmine Bromide1101

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDay 1 - No Drug
Total, all-cause mortalityDay 2 - Pyridostigmine Bromide
Total, other adverse eventsDay 1 - No Drug010
Total, other adverse eventsDay 2 - Pyridostigmine Bromide010
Total, serious adverse eventsDay 1 - No Drug010
Total, serious adverse eventsDay 2 - Pyridostigmine Bromide210

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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 comparisons1

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

Comparison
Day 1 - No Drug vs Day 2 - Pyridostigmine Bromide: serious adverse events

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/NCT02307526

GET https://conductscience.org/api/trials/v1/NCT02307526/registered