Myelodysplastic SyndromesNCT07570056
Use of Electrical Bioimpedance in Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS) Patients (Bioimpedance)
An observational study of Myelodysplastic Syndromes and Acute Myeloid Leukemia, run by University of Utah.
Trial summary
The goal of this project is to test non-invasive, painless skin electrical bioimpedance (BioZ) measurements as an adjunctive biomarker to standard bone marrow biopsies. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Myelodysplastic Syndromes, Acute Myeloid Leukemia
- What is being tested?
- Bioimpedance (BioZ)
- How many people
- 25 participants
- Where
- No sites listed yet
- Study dates
- Oct 2026to Jul 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with suspected or confirmed diagnosis of Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS)
Who may be able to join
- Suspected or confirmed diagnosis of Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS) and undergoing a bone marrow biopsy.
- Age 18 or older.
- Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.
Who cannot join
- Study prospect that has an electronic implant (cardiac, neurological, sensory, prosthetic implants with an electronic component. Also monitoring and drug delivery systems.)
- Medical, psychiatric, cognitive, or other conditions that may compromise the participant's ability to understand the participant information, give informed consent, comply with the study protocol or complete the study.
- Pregnant women
- Inability to understand and/or speak the English or Spanish language.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: A Pilot Study for the Use of Electrical Bioimpedance in Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS) Patients (Bioimpedance)
The goal of this project is to test non-invasive, painless skin electrical bioimpedance (BioZ) measurements as an adjunctive biomarker to standard bone marrow biopsies.
Read the detailed description
The goal of this project is to test non-invasive, painless skin electrical bioimpedance (BioZ) measurements as an adjunctive biomarker to standard bone marrow biopsies.
NIH NCI Surveillance, Epidemiology, and End Results Program estimates are that 22,010 new cases of acute myeloid leukemia (AML) will be diagnosed in 2025 with an estimated 11,090 AML-associated deaths, and an estimated 5-year relative survival of 32.9%. Recent progress has led to several new approvals in the first line or relapsed/refractory setting. Treatments usually consist of repeated cycles of chemotherapy, sometimes leading to a stem cell transplant. Yet, despite these advances, cure rates have remained at around 25 - 30%.
The main diagnostic procedure for AML and MDS is a bone marrow aspirate and biopsy (BMBX). The procedure is done using specialized biopsy needles that are pushed in the bone at the level of the posterior iliac crest under local anesthesia. The first step is to aspirate samples of the liquid marrow using a smaller needle. Once the needle is in place, syringes are used to aspirate liquid marrow. The aspiration step is usually uncomfortable irrespective of the level of local anesthesia. The second step of the procedure is to obtain a core biopsy. This is done using a larger needle (Jamshidi needle) that is pushed in the bone at the level of the posterior iliac crest. Once the needle is anchored in the bone, a core of the bone is cut out by rotating the needle over its axis. This is followed by "shaking" motions of the needle to dislodge the core from the bone. The Jamshidi needle is then slowly removed and the core collected for analysis. Samples obtained are analyzed for morphology to estimate bone marrow cellularity and leukemia cell count as well as flow cytometry and molecular diagnostics.
In general, patients have a BMBX at the time of initial diagnosis. Once treatment is started, another BMBX is frequently obtained 2 to 3 weeks after initiation of chemotherapy. A third BMBX is obtained at the time of recovery from the initial treatment cycle. Subsequently, additional BMBX procedures are done to rule out suspected relapses or before proceeding with another line of therapy, such as a bone marrow transplant. BMBX procedures are generally regarded as safe. There is not extensive literature on the incidence and severity of BMBX complications. These include bleeding (that can be serious in leukemic patients with compromised coagulation), infection, and potential nerve damage. A study surveying BMBX procedures in the United Kingdom reported a complication rate of less than 1%, most of which were hemorrhages3. However, in spite of local anesthesia, BMBX procedures can be traumatic and can be associated with significant discomfort with resultant distress to the patient. The procedure can be more traumatic in patients who are overweight or have brittle bones (such as patients with osteoporosis). Frequently, patients have to be put under sedation and have the procedure done under radiologic guidance in order to minimize distress or risks. Consequently, a non-invasive method to evaluate the bone marrow of AML and MDS patients is clearly needed.
Bioimpedance (BioZ) has been reported to be valuable in the detection of various cancers including skin, thyroid, liver, cervix, and breast cancers. Previous studies have shown that cancer tissue has unique electrical properties that are different from non-cancerous tissue. The BioZ device uses a low-intensity electrical current that is applied from inside of the BioZ device that has small electrodes at the tip. To interrogate these electrical properties, the electrodes (tip of the device) will be placed on the skin in the area of the hip. Once this occurs, the electrodes will be activated and the low-intensity current will be applied. As the current moves through the skin the device has a probe to detect changes in current that may be associated with cancer. Data from the probe is related to a secure phone that has an app to collect information. It will take about 1 minute to complete the measurement. The measurement will be completed 3 times. The presence of AML or MDS triggers a complex cascade of physiological changes within the tissue matrix, including alterations in interstitial fluids, lymphatic activity, as well as cellular and anatomical structures. By quantifying the skin electrical contrasts associated with these pathological changes, a non-invasive skin BioZ measurement at the level of the posterior iliac crest could have significant clinical value as a simple way to follow up AML or MDS patients throughout their treatment course. Here, the development of BioZ technology could provide an accurate biomarker of disease progression and treatment in AML and MDS and enable clinicians to detect and provide life-saving treatment for AML and MDS patients.
- Conditions
- Myelodysplastic Syndromes, Acute Myeloid Leukemia
- Being tested
- Bioimpedance (BioZ)
- Medical subject headings
- Myelodysplastic Syndromes, Leukemia, Myeloid, Acute
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Bioimpedance (BioZ)Diagnostic test
The BioZ device uses a low-intensity electrical current that is applied from inside of the BioZ device that has small electrodes at the tip. To interrogate these electrical properties, the electrodes (tip of the device) will be placed on the skin in the area of the hip. Once this occurs, the electrodes will be activated and the low-intensity current will be applied. As the current moves through the skin the device has a probe to detect changes in current that may be associated with cancer. Data from the probe is related to a secure phone that has an app to collect information.
| Study group | Role | What they receive |
|---|---|---|
| Patients with Suspected or AML or MDS | BioZ measurements will take about 1 minute to complete. The measurement will be completed 3 times. Receives: Diagnostic Test: Bioimpedance (BioZ) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlate BioZ findings with Pathologic Results
The primary outcome measure of this study is to correlate BioZ findings with pathologic results from bone marrow biopsies with AML or MDS.
Measured: up to one day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 May 2026
- Study startOct 2026 (estimated)
- Primary completionJul 2027 (estimated)
- Study completionJul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for Myelodysplastic SyndromesStudies of the same condition, open and under way.
- More trials run by University of UtahThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 25 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Utah
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Paul Shami, MD, Principal investigator, Huntsman Cancer Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07570056
- Sponsor's protocol ID
- 190884
- Status last verified
- Apr 2026
- First submitted
- 29 Apr 2026
- Last updated
- 30 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Talati C, Sweet K. Recently approved therapies in acute myeloid leukemia: A complex treatment landscape. Leuk Res. 2018 Oct;73:58-66. doi: 10.1016/j.leukres.2018.09.001. Epub 2018 Sep 8.
PubMed 30223250Bain BJ. Bone marrow biopsy morbidity: review of 2003. J Clin Pathol. 2005 Apr;58(4):406-8. doi: 10.1136/jcp.2004.022178.
PubMed 15790706Andreasen N, Crandall H, Brimhall O, Miller B, Perez-Tamayo J, Martinsen OG, Kauwe SK, Sanchez B. Skin Electrical Resistance as a Diagnostic and Therapeutic Biomarker of Breast Cancer Measuring Lymphatic Regions. IEEE Access. 2021;9:152322-152332. doi: 10.1109/access.2021.3123569. Epub 2021 Oct 27.
PubMed 34888126Luo X, Zhou Y, Smart T, Grossman D, Sanchez B. Electrical Characterization of Basal Cell Carcinoma Using a Handheld Electrical Impedance Dermography Device. JID Innov. 2021 Nov 26;2(1):100075. doi: 10.1016/j.xjidi.2021.100075. eCollection 2022 Jan.
PubMed 35072140Wen-Ying Wong E, Pandeya S, Crandall H, Smart T, Dixon M, Boucher KM, Florell SR, Grossman D, Sanchez B. Electrical Impedance Dermography Differentiates Squamous Cell Carcinoma In Situ from Inflamed Seborrheic Keratoses. JID Innov. 2023 Feb 20;3(3):100194. doi: 10.1016/j.xjidi.2023.100194. eCollection 2023 May.
PubMed 37066115Hansen NJ, Woodman K, Buoy S, Mao S, Barbon CEA, Lai SY, Fuller CD, Hutcheson KA, Sanchez B. Tongue electrical impedance myography correlates with functional, neurophysiologic, and clinical outcome measures in long-term oropharyngeal cancer survivors with and without hypoglossal neuropathy: An exploratory study. Head Neck. 2024 Mar;46(3):581-591. doi: 10.1002/hed.27618. Epub 2023 Dec 22.
PubMed 38133080
Study at a glance
From the registry record, last updated by the sponsor on 30 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Pilot Study for the Use of Electrical Bioimpedance in Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS) Patients (Bioimpedance)
- ClinicalTrials.gov ID
- NCT07570056
- Acronym / sponsor ID
- 190884
- Conditions
- Myelodysplastic Syndromes, Acute Myeloid Leukemia
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 25 participants (estimated)
- Lead sponsor
- University of UtahUniversity, hospital or other
- Study start
- Oct 2026 (estimated)
- Primary completion
- Jul 2027 (estimated)
- Study completion
- Jul 2027 (estimated)
- First posted
- 6 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this project is to test non-invasive, painless skin electrical bioimpedance (BioZ) measurements as an adjunctive biomarker to standard bone marrow biopsies.
Detailed description
The goal of this project is to test non-invasive, painless skin electrical bioimpedance (BioZ) measurements as an adjunctive biomarker to standard bone marrow biopsies.
NIH NCI Surveillance, Epidemiology, and End Results Program estimates are that 22,010 new cases of acute myeloid leukemia (AML) will be diagnosed in 2025 with an estimated 11,090 AML-associated deaths, and an estimated 5-year relative survival of 32.9%. Recent progress has led to several new approvals in the first line or relapsed/refractory setting. Treatments usually consist of repeated cycles of chemotherapy, sometimes leading to a stem cell transplant. Yet, despite these advances, cure rates have remained at around 25 - 30%.
The main diagnostic procedure for AML and MDS is a bone marrow aspirate and biopsy (BMBX). The procedure is done using specialized biopsy needles that are pushed in the bone at the level of the posterior iliac crest under local anesthesia. The first step is to aspirate samples of the liquid marrow using a smaller needle. Once the needle is in place, syringes are used to aspirate liquid marrow. The aspiration step is usually uncomfortable irrespective of the level of local anesthesia. The second step of the procedure is to obtain a core biopsy. This is done using a larger needle (Jamshidi needle) that is pushed in the bone at the level of the posterior iliac crest. Once the needle is anchored in the bone, a core of the bone is cut out by rotating the needle over its axis. This is followed by "shaking" motions of the needle to dislodge the core from the bone. The Jamshidi needle is then slowly removed and the core collected for analysis. Samples obtained are analyzed for morphology to estimate bone marrow cellularity and leukemia cell count as well as flow cytometry and molecular diagnostics.
In general, patients have a BMBX at the time of initial diagnosis. Once treatment is started, another BMBX is frequently obtained 2 to 3 weeks after initiation of chemotherapy. A third BMBX is obtained at the time of recovery from the initial treatment cycle. Subsequently, additional BMBX procedures are done to rule out suspected relapses or before proceeding with another line of therapy, such as a bone marrow transplant. BMBX procedures are generally regarded as safe. There is not extensive literature on the incidence and severity of BMBX complications. These include bleeding (that can be serious in leukemic patients with compromised coagulation), infection, and potential nerve damage. A study surveying BMBX procedures in the United Kingdom reported a complication rate of less than 1%, most of which were hemorrhages3. However, in spite of local anesthesia, BMBX procedures can be traumatic and can be associated with significant discomfort with resultant distress to the patient. The procedure can be more traumatic in patients who are overweight or have brittle bones (such as patients with osteoporosis). Frequently, patients have to be put under sedation and have the procedure done under radiologic guidance in order to minimize distress or risks. Consequently, a non-invasive method to evaluate the bone marrow of AML and MDS patients is clearly needed.
Bioimpedance (BioZ) has been reported to be valuable in the detection of various cancers including skin, thyroid, liver, cervix, and breast cancers. Previous studies have shown that cancer tissue has unique electrical properties that are different from non-cancerous tissue. The BioZ device uses a low-intensity electrical current that is applied from inside of the BioZ device that has small electrodes at the tip. To interrogate these electrical properties, the electrodes (tip of the device) will be placed on the skin in the area of the hip. Once this occurs, the electrodes will be activated and the low-intensity current will be applied. As the current moves through the skin the device has a probe to detect changes in current that may be associated with cancer. Data from the probe is related to a secure phone that has an app to collect information. It will take about 1 minute to complete the measurement. The measurement will be completed 3 times. The presence of AML or MDS triggers a complex cascade of physiological changes within the tissue matrix, including alterations in interstitial fluids, lymphatic activity, as well as cellular and anatomical structures. By quantifying the skin electrical contrasts associated with these pathological changes, a non-invasive skin BioZ measurement at the level of the posterior iliac crest could have significant clinical value as a simple way to follow up AML or MDS patients throughout their treatment course. Here, the development of BioZ technology could provide an accurate biomarker of disease progression and treatment in AML and MDS and enable clinicians to detect and provide life-saving treatment for AML and MDS patients.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients with Suspected or AML or MDS | – | Diagnostic Test: Bioimpedance (BioZ)BioZ measurements will take about 1 minute to complete. The measurement will be completed 3 times. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with suspected or confirmed diagnosis of Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS)
Key inclusion criteria (3 listed)
- Suspected or confirmed diagnosis of Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS) and undergoing a bone marrow biopsy.
- Age 18 or older.
- Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.
Key exclusion criteria (4 listed)
- Study prospect that has an electronic implant (cardiac, neurological, sensory, prosthetic implants with an electronic component. Also monitoring and drug delivery systems.)
- Medical, psychiatric, cognitive, or other conditions that may compromise the participant's ability to understand the participant information, give informed consent, comply with the study protocol or complete the study.
- Pregnant women
- Inability to understand and/or speak the English or Spanish language.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Bioimpedance (BioZ)The BioZ device uses a low-intensity electrical current that is applied from inside of the BioZ device that has small electrodes at the tip. To interrogate these electrical properties, the electrodes (tip of the device) will be placed on the skin in the area of the hip. Once this occurs, the electrodes will be activated and the low-intensity current will be applied. As the current moves through the skin the device has a probe to detect changes in current that may be associated with cancer. Data from the probe is related to a secure phone that has an app to collect information. | Diagnostic test | Patients with Suspected or AML or MDS |
Primary outcome
Correlate BioZ findings with Pathologic Results
Time frame: up to one day
The primary outcome measure of this study is to correlate BioZ findings with pathologic results from bone marrow biopsies with AML or MDS.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Sep 2026.
- Background: PubMed 30223250Talati C, Sweet K. Recently approved therapies in acute myeloid leukemia: A complex treatment landscape. Leuk Res. 2018 Oct;73:58-66. doi: 10.1016/j.leukres.2018.09.001. Epub 2018 Sep 8.
- Background: PubMed 15790706Bain BJ. Bone marrow biopsy morbidity: review of 2003. J Clin Pathol. 2005 Apr;58(4):406-8. doi: 10.1136/jcp.2004.022178.
- Background: PubMed 34888126Andreasen N, Crandall H, Brimhall O, Miller B, Perez-Tamayo J, Martinsen OG, Kauwe SK, Sanchez B. Skin Electrical Resistance as a Diagnostic and Therapeutic Biomarker of Breast Cancer Measuring Lymphatic Regions. IEEE Access. 2021;9:152322-152332. doi: 10.1109/access.2021.3123569. Epub 2021 Oct 27.
- Background: PubMed 35072140Luo X, Zhou Y, Smart T, Grossman D, Sanchez B. Electrical Characterization of Basal Cell Carcinoma Using a Handheld Electrical Impedance Dermography Device. JID Innov. 2021 Nov 26;2(1):100075. doi: 10.1016/j.xjidi.2021.100075. eCollection 2022 Jan.
- Background: PubMed 37066115Wen-Ying Wong E, Pandeya S, Crandall H, Smart T, Dixon M, Boucher KM, Florell SR, Grossman D, Sanchez B. Electrical Impedance Dermography Differentiates Squamous Cell Carcinoma In Situ from Inflamed Seborrheic Keratoses. JID Innov. 2023 Feb 20;3(3):100194. doi: 10.1016/j.xjidi.2023.100194. eCollection 2023 May.
- Background: PubMed 38133080Hansen NJ, Woodman K, Buoy S, Mao S, Barbon CEA, Lai SY, Fuller CD, Hutcheson KA, Sanchez B. Tongue electrical impedance myography correlates with functional, neurophysiologic, and clinical outcome measures in long-term oropharyngeal cancer survivors with and without hypoglossal neuropathy: An exploratory study. Head Neck. 2024 Mar;46(3):581-591. doi: 10.1002/hed.27618. Epub 2023 Dec 22.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Paul Shami, MD principal investigator
Huntsman Cancer Institute
Questions about this trial
What is this clinical trial studying?
An observational study of Myelodysplastic Syndromes and Acute Myeloid Leukemia, run by University of Utah.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 30 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Paul Shami, MD (801-585-5136, paul.shami@utah.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Correlate BioZ findings with Pathologic Results (time frame: up to one day). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07570056, which also lists 6 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2026.