CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 30 target
Drug / intervention
Conjugated Estrogen +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03663543
NCT03663543Phase 2ActiveOn TrackUpdated 2mo ago

The Use of Peri-Operative Intravenous Estrogen for the Mitigation of Ischemia Reperfusion Injury in the Setting of Renal Transplantation

University of Pennsylvania·interventional·Posted Sep 10, 2018·Updated Apr 16, 2026

In Brief

A Phase 2 clinical trial evaluating Conjugated Estrogen and Normal saline for Ischemia Reperfusion Injury. Active but no longer recruiting, targeting 30 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2Active
20172018201920202021202220232024202520262027
First PostedSep 10, 2018
Enrollment StartAug 26, 2016
Primary CompletionJan 31, 2027
Study CompletionMay 1, 2027
TodayJul 2, 2026
Enrollment to primary: 10.4 yearsPosted 7.8 years agoPrimary completion in 7 months

Interventions

Conjugated Estrogendrug

Dosing of conjugated estrogen will be given pre kidney transplant procedure and twice after reperfusion of the transplanted kidney.

Normal salinedrug

Dosing of normal saline will be given pre kidney transplant procedure and twice after reperfusion of the transplanted kidney.