ConductScience.org, home

Trial · NCT00511355

Registered outcomes47

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

ListOutcomeTime frameDescription
PrimarySerum Concentration of Prothrombin Fragments 1 + 2Baseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of D-DimerBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimaryActivated Protein C (APC) Resistance Ratio (Endogenous Thrombin Potential [ETP]-Based)Baseline and Cycle 6 (between Days 15 and 21 of the cycle)
Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). APC resistance ratio (ETP-based) measures the anticoagulation response of plasma to APC after activation of the extrinsic coagulation pathway. An increase in the ratio indicates a reduced responsiveness to APC. Each cycle consists of 28 days.
PrimarySerum Concentration of Clotting Factor VIIaBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Clotting Factor VIIcBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Clotting Factor VIIIBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Clotting Factor IIBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Antithrombin IIIBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Protein S (Free)Baseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Protein S (Total)Baseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Protein CBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimaryAPC Resistance Ratio (Activated Partial Thromboplastin Time [APTT]-Based)Baseline and Cycle 6 (between Days 15 and 21 of the cycle)
Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). APC resistance ratio (APTT-based) measures the anticoagulation response of plasma to APC after activation of the intrinsic coagulation pathway. An increase in the ratio indicates a increased responsiveness to APC. Each cycle consists of 28 days.
PrimarySerum Concentration of Sex Hormone Binding Globulin (SHBG)Baseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of C-Reactive Protein (CRP)Baseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Total CholesterolBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of High Density Lipoprotein (HDL)-CholesterolBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of HDL2-cholesterolBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of HDL3-cholesterolBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Low Density Lipoprotein (LDL)-CholesterolBaseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.
PrimarySerum Concentration of Apolipoprotein A-1Baseline and Cycle 6 (between Days 15 and 21 of the cycle)Serum samples were obtained under fasting conditions (no food or alcoholic beverages within 12 hours of serum sampling). Each cycle consists of 28 days.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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 list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT00511355/registered