CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 10 enrolled
Drug / intervention
Dalbavancin via Intravenous Administration +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/NCT02940730
NCT02940730Phase 4Completed

Evaluation of Intravenous and Intraperitoneal Pharmacokinetics of Dalbavancin in Peritoneal Dialysis Patients

University of Colorado, Denver·interventional·Posted Oct 21, 2016·Updated Mar 19, 2021

In Brief

A Phase 4 clinical trial evaluating Dalbavancin via Intravenous Administration and Dalbavancin via Intraperitoneal Administration for Infectious Peritonitis. Completed, enrolled 10 participants across 1 site.

Detailed Summary

This study will evaluate the pharmacokinetic properties of dalbavancin when administered as an intravenous infusion and instilled into the peritoneal space in patients who are undergoing peritoneal dialysis. The patients will receive intravenous dalbavancin followed by intensive plasma and peritoneal dialyses fluid sampling. Following a washout phase, the patients will then receive dalbavancin instilled into their peritoneal space followed by the same intensive plasma and peritoneal dialyses fluid sampling.

Study Details

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

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedOct 21, 2016
Enrollment StartMay 1, 2017
Primary CompletionJun 18, 2018
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 9.7 years ago

Interventions

Dalbavancin via Intravenous Administrationdrug

Patients will undergo plasma fluid pharmacokinetic sampling for determination of dalbavancin concentrations at time zero, 1 hour, 2 hours, 3 hours, 4 hours, 6 hours, at time of volume exchange.

Dalbavancin via Intraperitoneal Administrationdrug

Patients will undergo peritoneal fluid pharmacokinetic sampling for determination of dalbavancin concentrations at time zero, 1 hour, 2 hours, 3 hours, 4 hours, 6 hours, at time of volume exchange.