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NCT06686693 · ClinicalTrials.gov registry record · Phase 4

Intravenous Iron Effects on Performance at High Altitude

A Phase 4 study of Hypoxia, sponsored by United States Army Research Institute of Environmental Medicine.

Recruiting
Registry status
Phase 4
Development phase
24
Enrollment target
1
Study location

NCT06686693 is a Phase 4 study of Hypoxia that is actively recruiting participants, run by United States Army Research Institute of Environmental Medicine. The registered enrollment target is 24 participants, below the 3,116-participant average among 39 other Hypoxia trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06686693, a Phase 4 study of Hypoxia, is actively recruiting participants, sponsored by United States Army Research Institute of Environmental Medicine.

RECRUITING
Registry status
Phase 4
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

To compare the effects of IV iron versus placebo (saline) injection on arterial oxygen saturation, submaximal exercise responses, and 2-mile treadmill time-trial performance during acute exposure to hypobaric hypoxia (430 mmHg, simulating \~4800m) assessed 1 and 14 days after treatment. Primary Hypothesis 1: IV iron treatment will improve arterial oxygen saturation at rest and during exercise in acute hypobaric hypoxia and this effect will persist for 2 weeks Primary Hypothesis 2) IV iron treatment will improve 2-mile treadmill time trial performance in acute hypobaric hypoxia and this effect will persist for 2 weeks

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Injectafer

Study Locations (1)

Massachusetts

  • USARIEM - Natick

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2022-04-15
Est. Completion 2025-09-30
Phase Phase 4

What the Registry Record Tells You About NCT06686693

The ClinicalTrials.gov registry entry for NCT06686693 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,116-participant average among 39 other Hypoxia trials with a reported enrollment target (99% lower). The listed sponsor is United States Army Research Institute of Environmental Medicine, which has 59 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hypoxia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06686693 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT06686693 about?

NCT06686693 is a clinical study titled "Intravenous Iron Effects on Performance at High Altitude". To compare the effects of IV iron versus placebo (saline) injection on arterial oxygen saturation, submaximal exercise responses, and 2-mile treadmill time-trial performance during acute exposure to hypobaric hypoxia (430 mmHg, simulating \~4800m) assessed 1 and 14 days after treatment. Primary Hyp...

What is the current status of trial NCT06686693?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 24 participants. The study started on 2022-04-15. Estimated completion is 2025-09-30.

What conditions does trial NCT06686693 study?

This clinical trial studies the following conditions: Hypoxia.

What interventions are being tested in trial NCT06686693?

The interventions under investigation include: Placebo (OTHER), Injectafer (DRUG).

Who is sponsoring clinical trial NCT06686693?

This trial is sponsored by United States Army Research Institute of Environmental Medicine, which has 59 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06686693 being conducted?

This trial has 1 study location across Massachusetts. 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 Editorial

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