ClinicalTrials.gg
Active, not recruitingNCT06112236Updated Nov 1, 2023

Effects of Treatments for Anemia and Iron Deficiency on the Electrolyte Balance in Lung Transplant Recipients: A Special Focus on Hypophosphatemia

An observational study in Hypophosphatemia, sponsored by University of Zurich. Active, not recruiting at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-11-01.

Sponsored by University of Zurich · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
250
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to generate evidence regarding hypophosphatemia after iron infusion in lung transplant recipients in context of anemia and/or iron deficiency.

02

Conditions studied

  • Hypophosphatemia

Browse trials for

03

In context

Hypophosphatemia

53 studies on the registry are indexed under Hypophosphatemia; 16 are open to participants now.

This study's planned enrollment of 250 is above the median of 105 across 26 observational studies indexed under Hypophosphatemia.

Browse Hypophosphatemia studies →

Lead sponsor

University of Zurich is the lead sponsor of 1,049 studies on the registry; 133 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

lung transplant recipient

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • lung transplant recipient
  • treated at the University Hospital Zurich between 2015 until 2022

Exclusion criteria

Exclusion Criteria:

  • Denied general consent
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
250 participants (estimated)
Patient registry
No

Interventions

  • Otherno intervention

    no intervention

06

What researchers measure

Primary outcomes

  1. Change of serum phosphate level

    Change of serum phosphate level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

Secondary outcomes

  1. Change of urin phosphate level

    Change of urin phosphate level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  2. Change of hemoglobin

    Change of hemoglobin level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  3. Change of mean corpuscular volume (MCV)

    Changes of serum MCV level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  4. Change of mean corpuscular hemoglobin (MCH)

    Change of serum MCH level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  5. Change of serum magnesium

    Change of serum magnesium level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  6. Change of serum and urin calcium

    Change of serum and urin calcium level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  7. Change of serum albumin

    Change of serum albumin level before and after iron infusion

    Time frame: Baseline and up to 90 days after iron infusion

  8. Complications after iron infusion

    Number of patients with complications due to hypophosphatemia after iron infusion (Hospitalization, hypoxia, fracture due to hypophosphatemia)

    Time frame: 2015-2022

  9. Predictors

    Analysis of possible predictors for the decrease of serum phosphate levels after iron infusion

    Time frame: baseline and up to 90 days after iron infusion

  10. Therapeutic management

    Descriptive analysis of therapeutic management of hypophosphatemia after iron infusion

    Time frame: 2015 to 2022

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06112236
Responsible party
Sponsor
First posted
Nov 1, 2023
Start date
Feb 17, 2023
Primary completion
Dec 31, 2026 (estimated)
Completion
Mar 31, 2027 (estimated)
Last update
Nov 1, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion