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Trial · NCT00228267

Propofol Injection for Daily Headache

NCT00228267, Phase 2, Completed, University of Alberta

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Propofol Injection for Daily Headache. Trials, record NCT00228267. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00228267

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Trial

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

Title
Propofol Injection for Daily Headache
NCT number
NCT00228267
Status
Completed
Phases
Phase 2
Enrollment
28 participants, estimated
Lead sponsor
University of Alberta
Conditions
Chronic Headache, Analgesic Rebound Headache, Chronic Daily Headache, Headache, Intractable
Interventions
Propofol
First posted
2005-09-28
Last updated
2017-05-04

Source ClinicalTrials.gov

Registered outcomes9

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

ListOutcomeTime frameDescription
PrimaryHeadache Disability Index and the Headache Index
Primary
The baseline Headache Index is the mean of all 28 NRS pain scores (four measures daily for seven days) and the post-treatment Headache Index is the mean of all 120 NRS pain scores (four measures daily for thirty days)
SecondaryNumber of days with a headache of at least moderate severity defined as pain at least 5 on the Numerical Rating Scale (NRS).
SecondaryPeak daily headache severity according to the NRS.
Secondary
Analgesic medication consumption will be measured in terms of morphine equivalents of narcotic medication and number of tablets /doses of acetaminophen / non-steroidal anti-inflammatory (NSAID) containing analgesics.53
SecondaryVisits to the Emergency Room for headache treatment.
SecondarySedation and nausea scores in the treatment and placebo groups.
SecondaryAbility of participants in each of the groups to correctly guess their treatment assignment.
SecondaryAdverse effects related to the infusion

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

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 totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
19923528RESULT

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/NCT00228267

GET https://conductscience.org/api/trials/v1/NCT00228267/registered