Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03412045 · ClinicalTrials.gov registry record · NA

Hyperbaric Oxygen Therapy in Sickle Cell Pain

A NA study, sponsored by University of Nebraska.

Completed
Registry status
NA
Development phase
8
Enrollment target

NCT03412045: Completed NA study, sponsored by University of Nebraska.

NCT03412045 is a NA study that has completed, run by University of Nebraska. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03412045, a NA study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

Sickle cell anemia is a genetic blood disorder where red blood cells are abnormally shaped, crescent- or sickle-shaped, instead of the normal, round shape. This misshapen cell is rigid and sticky, causing them to clump together and block small blood vessels. This blockage can lead to pain, infections, and organ damage, and the shortened lifespan of sickle cells causes anemia. The purpose of this study is to explore if hyperbaric oxygen (HBO) therapy would decrease pain and hospital length of stay associated with acute sickle cell pain crisis. Adults presenting with an uncomplicated acute pain crisis (i.e., acute chest syndrome, acute myocardial infarction/stroke) would be eligible. The intervention would be 1-3 hyperbaric oxygen sessions depending on response to therapy. Each treatment session will be approximately two hours in length. Evaluation would be through participants' self--assessment via the visual analog scale for pain level before and after treatments as well as tracking length of stay in the hospital.

Primary Outcome

Comparison of total analgesic administered to patient during control hospital stay versus intervention HBO treatment hospital stay. Each patient serves as their own control. The patient receives HBO treatment during one hospital admission, and the amount of analgesic received is compared to the patient's previous hospital admission.

Interventions

  • DEVICE hyperbaric oxygen therapy

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2022-09-01
Est. Completion 2025-06-05
Phase NA
University of Nebraska

407 total trials

What the finished NCT03412045 record still lists

NCT03412045 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which hyperbaric oxygen therapy is the first listed.

NCT03412045 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03412045 about?

NCT03412045 is a clinical study titled "Hyperbaric Oxygen Therapy in Sickle Cell Pain". Sickle cell anemia is a genetic blood disorder where red blood cells are abnormally shaped, crescent- or sickle-shaped, instead of the normal, round shape. This misshapen cell is rigid and sticky, causing them to clump together and block small blood vessels. This blockage can lead to pain, infection...

What is the current status of trial NCT03412045?

This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2022-09-01. Estimated completion is 2025-06-05.

What interventions are being tested in trial NCT03412045?

The interventions under investigation include: hyperbaric oxygen therapy (DEVICE).

Who is sponsoring clinical trial NCT03412045?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03412045's enrollment target sits among peer trials

8 1976th of 2000 higher than 19 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03412045, the US trial registry maintained by the National Library of Medicine. NCT03412045 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.