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

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, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

GFR (glomerular filtration rate) as calculated from a DTPA (Diethylenetriamine Pentaacetic Acid, a medication) renal scan.

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
University of Pennsylvania

1,423 total trials

What the registry record for NCT03663543 still lists

NCT03663543 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

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 a single indexed study location in 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.

Similar trials for Ischemia Reperfusion Injury

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03663543's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03663543, the US trial registry maintained by the National Library of Medicine. NCT03663543 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.