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

NCT07386548 · ClinicalTrials.gov registry record · NA

Biologic Injection For Adults With Lumbar Disc Herniation

A NA study, sponsored by Weill Medical College of Cornell University.

Not yet
Registry status
NA
Development phase
90
Enrollment target

NCT07386548: Clinical Trial NA study, sponsored by Weill Medical College of Cornell University.

NCT07386548 is a NA study that has not yet begun recruiting, run by Weill Medical College of Cornell University. The registered enrollment target is 90 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07386548, a NA study, has not yet begun recruiting, sponsored by Weill Medical College of Cornell University.

NOT YET RECRUITING
Registry status
NA
Development phase
90 participants
Enrollment target

Study Summary

The goal of this clinical trial is to find out whether adding a bone-marrow aspirate concentrate (BMAC) injection during surgery can improve recovery in adults undergoing lumbar microdiscectomy for a lumbar disc herniation. The main questions it aims to answer are: * Does the BMAC injection lead to better disc tissue health after surgery (as seen on MRI scans)? * Does the BMAC injection lead to greater improvement in pain and disability compared to surgery alone? Participants will be adults aged 18 and older who are scheduled for lumbar microdiscectomy surgery. Researchers will compare one group of participants receiving the standard-of-care surgery plus the BMAC injection with another group receiving the same surgery without the injection to see if the injection offers added benefit. Participants will: * Have surgery (microdiscectomy) with or without the injection. * Complete pain and disability questionnaires at several times over 2 years. * Undergo MRI scans at baseline and follow-up to assess disc structure and tissue health. * Provide samples of leftover disc or bone-marrow tissue (as applicable) from surgery for analysis.

Primary Outcome

MRI T2 mapping and T2 relaxation time are advanced imaging techniques that help assess the hydration status of intervertebral discs. These two metrics will be combined as one data point. T2 relaxation time measures the decay of the MRI signal, which is influenced by the water content in the disc. Higher T2 values indicate better hydration, while lower T2 values suggest dehydration and degeneration. T2 mapping provides a detailed, quantitative assessment of the disc's water content, allowing for

Interventions

  • OTHER Bone Marrow Aspirate Concentrate (BMAC)

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2026-05-01
Est. Completion 2030-12
Phase NA

What is known before NCT07386548 opens enrollment

NCT07386548 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which Bone Marrow Aspirate Concentrate (BMAC) is the first listed.

NCT07386548 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07386548 about?

NCT07386548 is a clinical study titled "Biologic Injection For Adults With Lumbar Disc Herniation". The goal of this clinical trial is to find out whether adding a bone-marrow aspirate concentrate (BMAC) injection during surgery can improve recovery in adults undergoing lumbar microdiscectomy for a lumbar disc herniation. The main questions it aims to answer are: * Does the BMAC injection lead t...

What is the current status of trial NCT07386548?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2026-05-01. Estimated completion is 2030-12.

What interventions are being tested in trial NCT07386548?

The interventions under investigation include: Bone Marrow Aspirate Concentrate (BMAC) (OTHER).

Who is sponsoring clinical trial NCT07386548?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07386548's enrollment target sits among peer trials

90 941st of 2000 higher than 1,029 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

  • NCT02521311 · 90 participants · Phase 2

    Assessment of Clemastine Fumarate as a Remyelinating Agent in Acute Optic Neuritis (ReCOVER)

  • NCT02939573 · 90 participants · Phase 2

    A Randomized Multicenter Study for Isolated Skin Vasculitis

  • NCT03128879 · 90 participants · Phase 2

    Venetoclax With Ibrutinib or Acalabrutinib in Pts. With High-risk CLL

  • NCT03184038 · 90 participants · NA

    Neurocognition in Patients With Multiple Brain Metastases Treated With Radiosurgery

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 NCT07386548, the US trial registry maintained by the National Library of Medicine. NCT07386548 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.