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NCT03663543 · ClinicalTrials.gov registry record · Phase 1

Intravenous Estrogen in Kidney Transplant Study

A Phase 1 study of Ischemia Reperfusion Injury, sponsored by University of Pennsylvania.

Active
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT03663543 is a Phase 1 study of Ischemia Reperfusion Injury that is active but no longer recruiting, run by University of Pennsylvania. The registered enrollment target is 30 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT03663543, a Phase 1 study of Ischemia Reperfusion Injury, is active but no longer recruiting, sponsored by University of Pennsylvania.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

Ischemia perfusion injury (IRI) is a major cause of organ injury during kidney transplantation. Currently there are no treatments for IRI other than dialysis. Preliminary studies in female mice have found protection from IRI when given short term estrogen supplements. This study will look at the effect of intravenous estrogen given peri-operatively to reduce the effect of IRI in female kidney transplant recipients.

Interventions

  • DRUG Normal saline
  • DRUG Conjugated Estrogen

Study Locations (1)

Pennsylvania

  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2016-08-26
Est. Completion 2026-05-01
Phase Phase 1

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT03663543

The ClinicalTrials.gov registry entry for NCT03663543 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Ischemia Reperfusion Injury appearing as the primary indexed condition, and to 2 interventions - of which Normal saline is the first listed.

NCT03663543 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT03663543 about?

NCT03663543 is a clinical study titled "Intravenous Estrogen in Kidney Transplant Study". Ischemia perfusion injury (IRI) is a major cause of organ injury during kidney transplantation. Currently there are no treatments for IRI other than dialysis. Preliminary studies in female mice have found protection from IRI when given short term estrogen supplements. This study will look at the eff...

What is the current status of trial NCT03663543?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2016-08-26. Estimated completion is 2026-05-01.

What conditions does trial NCT03663543 study?

This clinical trial studies the following conditions: Ischemia Reperfusion Injury.

What interventions are being tested in trial NCT03663543?

The interventions under investigation include: Normal saline (DRUG), Conjugated Estrogen (DRUG).

Who is sponsoring clinical trial NCT03663543?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03663543 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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