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Trial · NCT03449251

A Series of Pilot Studies to Evaluate the haemoDynamic and mEtabolic Effects oF apelIn aNd rElaxin

NCT03449251, Phase 2, Active not recruiting, Cambridge University Hospitals NHS Foundation Trust

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Series of Pilot Studies to Evaluate the haemoDynamic and mEtabolic Effects oF apelIn aNd rElaxin. Trials, record NCT03449251. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03449251

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Trial

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

Title
A Series of Pilot Studies to Evaluate the haemoDynamic and mEtabolic Effects oF apelIn aNd rElaxin
NCT number
NCT03449251
Status
Active not recruiting
Phases
Phase 2
Enrollment
170 participants, estimated
Lead sponsor
Cambridge University Hospitals NHS Foundation Trust
Conditions
Cardiovascular Diseases, Type 2 Diabetes Mellitus
Interventions
Apelin, Relaxin, Normal saline, Verapamil, LN Monomethyl arginine
First posted
2018-02-28
Last updated
2026-09-30

Source ClinicalTrials.gov

Registered outcomes58

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

ListOutcomeTime frameDescription
PrimarySub-study 1a: Changes in markers of glucose homeostasis in healthy participants after infusion of apelin (Glucose)Visit 2 to visit 4, over a period of up to 8 weeksGlucose, in mmol/l
PrimarySub-study 1a: Changes in markers of glucose homeostasis in healthy participants after infusion of apelin (C-Peptide)Visit 2 to visit 4, over a period of up to 8 weeksC-peptide, in pmol/L
PrimarySub-study 1a: Changes in markers of glucose homeostasis in healthy participants after infusion of apelin (Glucagon)Visit 2 to visit 4, over a period of up to 8 weeksGlucagon, in pg/ml
PrimarySub-study 1a: Changes in markers of glucose homeostasis in healthy participants after infusion of apelin (Insulin)Visit 2 to visit 4, over a period of up to 8 weeksInsulin, in pmol/L
PrimarySub-study 1a: Changes in markers of glucose homeostasis in healthy participants after infusion of apelin (TNF-alpha)Visit 2 to visit 4, over a period of up to 8 weeksTNF-alpha, in pg/ml
Primary
Sub-study 1b: Changes in markers of glucose homeostasis in participants with increased weight and participants with type 2 diabetes mellitus after infusion of apelin with or without mixed meal tolerance in obese/overweight and T2DM participants
Visit 2 to visit 5, over a period of up to 14 weeksGlucose, in mmol/l
Primary
Sub-study 1b: Changes in markers of glucose homeostasis in participants with increased weight and participants with type 2 diabetes mellitus after infusion of apelin with or without mixed meal tolerance in obese/overweight and T2DM participants
Visit 2 to visit 5, over a period of up to 14 weeksC-peptide, in pmol/L
Primary
Sub-study 1b: Changes in markers of glucose homeostasis in participants with increased weight and participants with type 2 diabetes mellitus after infusion of apelin with or without mixed meal tolerance in obese/overweight and T2DM participants
Visit 2 to visit 5, over a period of up to 14 weeksGlucagon, in pg/ml
Primary
Sub-study 1b: Changes in markers of glucose homeostasis in participants with increased weight and participants with type 2 diabetes mellitus after infusion of apelin with or without mixed meal tolerance in obese/overweight and T2DM participants
Visit 2 to visit 5, over a period of up to 14 weeksInsulin, in pmol/L
Primary
Sub-study 1b: Changes in markers of glucose homeostasis in participants with increased weight and participants with type 2 diabetes mellitus after infusion of apelin with or without mixed meal tolerance in obese/overweight and T2DM participants
Visit 2 to visit 5, over a period of up to 14 weeksTNF-alpha, in pg/ml

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.

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/NCT03449251

GET https://conductscience.org/api/trials/v1/NCT03449251/registered?page=2