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Trial · NCT03720990

Smith-Lemli-Opitz Syndrome and Cholic Acid

NCT03720990, Phase 1, Phase 2, Completed, University of Nebraska; results first posted 2023-12-13

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Smith-Lemli-Opitz Syndrome and Cholic Acid. Trials, record NCT03720990. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03720990

On this page

Trial

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

Title
Smith-Lemli-Opitz Syndrome and Cholic Acid
NCT number
NCT03720990
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
12 participants, actual
Lead sponsor
University of Nebraska
Conditions
Smith-Lemli-Opitz Syndrome
Interventions
Cholic Acid
First posted
2018-10-26
Last updated
2024-04-30
Results first posted
2023-12-13
Limitations and caveats
No limitations or caveats.

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryChange in Plasma Cholesterol8 weeksPlasma cholesterol will be measured. Response to cholic acid treatment will consist of a change in plasma cholesterol.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Plasma Cholesterol8 weekschange (%) compared to baselineMEAN

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Change in Plasma CholesterolCholic Acid37.8Standard Deviation 22.4change (%) compared to baseline

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCholic Acid12
Overall StudyCOMPLETEDCholic Acid12
Overall StudyNOT COMPLETEDCholic Acid0

Adverse events0

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

None in this release.

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCholic Acid012
Total, other adverse eventsCholic Acid012
Total, serious adverse eventsCholic Acid012

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 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/NCT03720990

GET https://conductscience.org/api/trials/v1/NCT03720990/registered