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

NCT01630707 · ClinicalTrials.gov registry record · NA

Evaluation of the Delivery of Optimized Supersaturated Oxygen Therapy to Treat Patients With an Acute Heart Attack

A NA study, sponsored by TherOx.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT01630707: Completed NA study, sponsored by TherOx.

NCT01630707 is a NA study that has completed, run by TherOx. The registered enrollment target is 20 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

NCT01630707, a NA study, has completed, sponsored by TherOx.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the feasibility of the delivery of SuperSaturated Oxygen (SSO2) Therapy for 60 minutes selectively into the left main coronary artery (LMCA). The therapy will be delivered with a commercially available qualified SSO2 delivery catheter used with the TherOx® DownStream® System and Cartridge in the treatment of patients presenting with an anterior acute myocardial infarction (heart attack) ≤ six hours after symptom onset with successful reperfusion (via PCI).

Primary Outcome

Successful administration of SSO2 Therapy (60 minutes) without dislodgment of the SSO2 delivery catheter during the infusion and without untoward Serious Adverse Events

Interventions

  • DEVICE SuperSaturated Oxygen (SS02) Therapy

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2012-08
Est. Completion 2014-08
Phase NA
TherOx

6 total trials

What the finished NCT01630707 record still lists

NCT01630707 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 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 SuperSaturated Oxygen (SS02) Therapy is the first listed.

NCT01630707 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01630707 about?

NCT01630707 is a clinical study titled "Evaluation of the Delivery of Optimized Supersaturated Oxygen Therapy to Treat Patients With an Acute Heart Attack". The purpose of this study is to evaluate the feasibility of the delivery of SuperSaturated Oxygen (SSO2) Therapy for 60 minutes selectively into the left main coronary artery (LMCA). The therapy will be delivered with a commercially available qualified SSO2 delivery catheter used with the TherOx® Do...

What is the current status of trial NCT01630707?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2012-08. Estimated completion is 2014-08.

What interventions are being tested in trial NCT01630707?

The interventions under investigation include: SuperSaturated Oxygen (SS02) Therapy (DEVICE).

Who is sponsoring clinical trial NCT01630707?

This trial is sponsored by TherOx, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01630707's enrollment target sits among peer trials

20 1768th of 2000 higher than 140 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 enrollment target

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01630707, the US trial registry maintained by the National Library of Medicine. NCT01630707 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.