Hereditary DiseasesNCT07718971
UW ISeqU: Clinical Impact of Whole-genome Sequencing in Adults
An observational study of Hereditary Diseases and Critical Illness, run by University of Washington at 1 site in United States.
Trial summary
The goal of this study is to learn how clinical whole genome sequencing can help identify diagnoses and guide medical care in adults. The study is based on the hypothesis that genome sequencing will identify a genetic explanation in some adults whose condition has not previously been diagnosed and that some results… Read more about this study
- Who is it for?
- Ages 18 to 50 years
- Conditions the study is for
- Hereditary Diseases, Critical Illness
- What is being tested?
- Genome sequencing
- How many people
- 1,000 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Jul 2026to 1 Jul 2032
- 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 to 50 years
- All sexes
- No healthy volunteers
- Adult
Study population: University of Washington - Montlake Campus or Harborview Medical Center Seattle, WA, USA
Who may be able to join
- Person has a medical condition that does not yet have a clear explanation
- Enough medical information is available within the UW Medicine system to evaluate the person's condition and interpret genetic test results
- A blood sample or cheek-swab sample can be collected for genetic testing
- The person does not already have a confirmed genetic diagnosis that fully explains their current medical condition
- The person, or their legally authorized representative when applicable, is willing and able to provide informed consent.
Who cannot join
- The current illness has a clear non-genetic explanation, such as a traumatic injury, confirmed overdose or intoxication, or an infection that fully explains the illness
- The person previously had genetic testing specifically for the current condition or symptoms, including prior whole-exome or whole-genome sequencing
- The person is currently incarcerated.
- The person has had a donor stem cell, bone marrow transplant or active blood cancer that makes a sample unsuitable for testing their inherited genetic information
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
University of Washington Medical Center
Seattle, Washington, 98195
About this study
The goal of this study is to learn how clinical whole genome sequencing can help identify diagnoses and guide medical care in adults. The study is based on the hypothesis that genome sequencing will identify a genetic explanation in some adults whose condition has not previously been diagnosed and that some results will change medical care. The main questions it aims to answer are:
- How often does genome sequencing identify a genetic diagnosis that explains or contributes to a participant's symptoms?
- How do genetic results affect medical care and decision-making?
- Is genome sequencing feasible and acceptable to adult patients and families?
- Are there differences in access to genetic testing or diagnosis across different groups of patients?
Read more
Participants will:
- Provide a blood sample (often collected during routine care) or cheek swab for genetic testing
- Allow researchers to review their medical records
- Receive genetic results that will also be shared with their medical team
- May be asked to complete a brief survey or interview about their experience
Researchers will follow participants over time to understand how genetic testing impacts diagnosis and care.
Read the detailed description
This is a prospective observational cohort study evaluating the use of clinical whole genome sequencing in adults with unexplained medical conditions, atypical disease courses, or clinical presentations for which a genetic contribution is suspected. Participants will be identified at the University of Washington Medicine sites (UW Montlake and Harborview Medical Center). The study is intended to characterize how genome sequencing can be incorporated into adult clinical care. Participation is voluntary and does not replace standard diagnostic evaluation or treatment.
Potential participants will be identified through review of hospital admissions and referrals from treating clinicians or specialty services. Informed consent may be completed in person, by telephone, or by secure videoconference. When a hospitalized participant is unable to provide consent because of illness or impaired decision-making capacity, consent may be obtained from a legally authorized representative in accordance with applicable requirements. During consent, participants will indicate whether they wish to receive ACMG medically actionable secondary findings and whether they agree to future contact.
After enrollment, the study team will collect clinical and phenotypic information relevant to genomic interpretation. Information may include the participant's presenting symptoms, medical and family history, prior diagnostic testing, medications, hospital course, and subsequent clinical care. Data will be obtained from participant or family interview, review of the electronic health record, and communication with the treating team. Clinical information from before and after sequencing will be collected to support interpretation and to evaluate the downstream effects of genomic findings.
The only physical procedure is collection of a biospecimen for genomic testing. Research blood collection will be coordinated with a clinically indicated blood draw to avoid an additional venipuncture. Alternatively, a buccal swab may be used.
A close biological relative may also be enrolled as a genetic comparator when this would assist in genetic interpretation. Comparator participation is optional. Comparators will provide a buccal specimen and limited identifying information needed for laboratory testing. Their medical records will not be reviewed.
Whole-genome sequencing will be performed and interpreted by GeneDx, a CLIA-certified laboratory. Variants will be classified using current ACMG/AMP standards. Findings will be assessed in relation to the participant's phenotype and may be categorized as diagnostic, contributory, secondary, or non-contributory. Variants of uncertain significance may be reported when considered relevant by the clinical laboratory.
Participants may choose whether to receive medically actionable secondary findings in genes recommended by the ACMG. Comparator analysis will generally be limited to variants relevant to interpretation of the enrolled participant. A comparator may receive a result when a clinically significant variant identified in the participant is also present in the comparator or when the comparator has separately chosen to receive an eligible secondary finding.
Clinically relevant results will be returned by a genetic counselor or clinical geneticist by telephone, secure video visit, or in person. Results will be communicated to the clinical team and will be made available in the medical record. When appropriate, participants may be advised to discuss additional evaluation, surveillance, treatment, or family testing with their clinicians or to seek consultation with a medical genetics referral. Clinical care resulting from a genomic finding, including laboratory testing, imaging, specialist referral, or treatment, is not provided as a study procedure.
In addition to the clinical laboratory analysis, genomic and clinical data may be used for exploratory research. These analyses may include pharmacogenomic assessment, evaluation of gene-disease relationships, or other studies of disease mechanisms and treatment response. Exploratory research findings will not be returned clinically.
The study team will review participants' medical records for up to 3 years after enrollment to evaluate the downstream clinical effects of sequencing, including changes in diagnosis, treatment, surveillance, referrals, and family counseling. Participants may also be invited to complete a brief survey or interview about their experience with genetic testing and result disclosure. Participants who agree to future contact may be contacted if clinically important new information or a meaningful reinterpretation of their genomic findings becomes available.
Clinical and genomic data will be stored using coded study identifiers on secure systems. The linkage between study identifiers and participant identities will be maintained separately, with access restricted to authorized study personnel. Genomic data may be retained for future reanalysis as scientific knowledge changes. Individual genetic variants may be submitted in de-identified form to public variant databases such as ClinVar; raw genomic data and medical records will not be included in those submissions.
- Conditions
- Hereditary Diseases, Critical Illness
- Being tested
- Genome sequencing
- Keywords
- genetic, genome sequencing, rapid whole genome sequencing, adult genetics, undiagnosed disease, critical illness genetics
- Medical subject headings
- Genetic Diseases, Inborn, Critical Illness, Undiagnosed Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Genome sequencingGenetic
Clinical whole-genome sequencing of blood or buccal DNA, with optional family comparator analysis and return of clinical results
| Study group | Role | What they receive |
|---|---|---|
| Adults Undergoing Clinical Genome Sequencing | Adults with unexplained medical conditions or clinical presentations who undergo clinical genome sequencing and longitudinal follow-up Receives: Genetic: Genome sequencing |
What is being measured
The primary outcome is the main question the study is designed to answer.
Diagnostic Yield of Clinical Genome Sequencing
Number and percentage of participants with one or more definitive or possible diagnostic findings on clinical genome sequencing. This will be further stratified as secondary outcome measures by clinical and demographic characteristics.
Measured: Through study completion, an average of 3 years
Secondary outcomes (1)
Short-term and long-term changes in medical management
Number and percentage of participants with a change in medical management attributable to the genome sequencing result. Changes may include initiation, discontinuation, or modification of medication or treatment; additional diagnostic testing; changes in monitoring or surveillance; inpatient consultation; outpatient referral; transition to comfort-focused care; or testing and evaluation of biological relatives.
Measured: At 6 months after testing and at 3 years after testing
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jul 2026
- Study start1 Jul 2026
- Primary completion1 Jul 2029 (estimated)
- Study completion1 Jul 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hereditary DiseasesStudies of the same condition, open and under way.
- More trials run by University of WashingtonThe 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
- 1,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Washington
- Sponsor type
- University, hospital or other
- Collaborators
- GeneDx
- Responsible party
- Principal investigator, Evonne McArthur, University of Washington
- Investigators
- Evonne McArthur, MD, PhD, Principal investigator, University of WashingtonDanny E Miller, MD, PhD, Study director, University of Washington
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07718971
- Sponsor's protocol ID
- STUDY00025204
- Other IDs
- RG1126449
- Status last verified
- Jul 2026
- First submitted
- 14 Jul 2026
- Last updated
- 22 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be made publicly available because the dataset includes sensitive clinical and genomic information. Aggregate study results may be shared through publications and presentations, and de-identified individual genetic variants may be submitted to public variant databases.
Study at a glance
From the registry record, last updated by the sponsor on 22 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- UW ISeqU: Clinical Impact of Whole-genome Sequencing in Adults
- ClinicalTrials.gov ID
- NCT07718971
- Acronym / sponsor ID
- STUDY00025204
- Conditions
- Hereditary Diseases, Critical Illness
- Keywords
- genetic, genome sequencing, rapid whole genome sequencing, adult genetics, undiagnosed disease, critical illness genetics
- Study type
- Observational
- Recruitment status
- Enrolling by invitation
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- University of WashingtonUniversity, hospital or other
- Collaborators
- GeneDx
- Study start
- 1 Jul 2026 (actual)
- Primary completion
- 1 Jul 2029 (estimated)
- Study completion
- 1 Jul 2032 (estimated)
- First posted
- 22 Jul 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 study is to learn how clinical whole genome sequencing can help identify diagnoses and guide medical care in adults. The study is based on the hypothesis that genome sequencing will identify a genetic explanation in some adults whose condition has not previously been diagnosed and that some results will change medical care. The main questions it aims to answer are:
- How often does genome sequencing identify a genetic diagnosis that explains or contributes to a participant's symptoms?
- How do genetic results affect medical care and decision-making?
- Is genome sequencing feasible and acceptable to adult patients and families?
- Are there differences in access to genetic testing or diagnosis across different groups of patients?
Participants will:
- Provide a blood sample (often collected during routine care) or cheek swab for genetic testing
- Allow researchers to review their medical records
- Receive genetic results that will also be shared with their medical team
- May be asked to complete a brief survey or interview about their experience
Researchers will follow participants over time to understand how genetic testing impacts diagnosis and care.
Detailed description
This is a prospective observational cohort study evaluating the use of clinical whole genome sequencing in adults with unexplained medical conditions, atypical disease courses, or clinical presentations for which a genetic contribution is suspected. Participants will be identified at the University of Washington Medicine sites (UW Montlake and Harborview Medical Center). The study is intended to characterize how genome sequencing can be incorporated into adult clinical care. Participation is voluntary and does not replace standard diagnostic evaluation or treatment.
Potential participants will be identified through review of hospital admissions and referrals from treating clinicians or specialty services. Informed consent may be completed in person, by telephone, or by secure videoconference. When a hospitalized participant is unable to provide consent because of illness or impaired decision-making capacity, consent may be obtained from a legally authorized representative in accordance with applicable requirements. During consent, participants will indicate whether they wish to receive ACMG medically actionable secondary findings and whether they agree to future contact.
After enrollment, the study team will collect clinical and phenotypic information relevant to genomic interpretation. Information may include the participant's presenting symptoms, medical and family history, prior diagnostic testing, medications, hospital course, and subsequent clinical care. Data will be obtained from participant or family interview, review of the electronic health record, and communication with the treating team. Clinical information from before and after sequencing will be collected to support interpretation and to evaluate the downstream effects of genomic findings.
The only physical procedure is collection of a biospecimen for genomic testing. Research blood collection will be coordinated with a clinically indicated blood draw to avoid an additional venipuncture. Alternatively, a buccal swab may be used.
A close biological relative may also be enrolled as a genetic comparator when this would assist in genetic interpretation. Comparator participation is optional. Comparators will provide a buccal specimen and limited identifying information needed for laboratory testing. Their medical records will not be reviewed.
Whole-genome sequencing will be performed and interpreted by GeneDx, a CLIA-certified laboratory. Variants will be classified using current ACMG/AMP standards. Findings will be assessed in relation to the participant's phenotype and may be categorized as diagnostic, contributory, secondary, or non-contributory. Variants of uncertain significance may be reported when considered relevant by the clinical laboratory.
Participants may choose whether to receive medically actionable secondary findings in genes recommended by the ACMG. Comparator analysis will generally be limited to variants relevant to interpretation of the enrolled participant. A comparator may receive a result when a clinically significant variant identified in the participant is also present in the comparator or when the comparator has separately chosen to receive an eligible secondary finding.
Clinically relevant results will be returned by a genetic counselor or clinical geneticist by telephone, secure video visit, or in person. Results will be communicated to the clinical team and will be made available in the medical record. When appropriate, participants may be advised to discuss additional evaluation, surveillance, treatment, or family testing with their clinicians or to seek consultation with a medical genetics referral. Clinical care resulting from a genomic finding, including laboratory testing, imaging, specialist referral, or treatment, is not provided as a study procedure.
In addition to the clinical laboratory analysis, genomic and clinical data may be used for exploratory research. These analyses may include pharmacogenomic assessment, evaluation of gene-disease relationships, or other studies of disease mechanisms and treatment response. Exploratory research findings will not be returned clinically.
The study team will review participants' medical records for up to 3 years after enrollment to evaluate the downstream clinical effects of sequencing, including changes in diagnosis, treatment, surveillance, referrals, and family counseling. Participants may also be invited to complete a brief survey or interview about their experience with genetic testing and result disclosure. Participants who agree to future contact may be contacted if clinically important new information or a meaningful reinterpretation of their genomic findings becomes available.
Clinical and genomic data will be stored using coded study identifiers on secure systems. The linkage between study identifiers and participant identities will be maintained separately, with access restricted to authorized study personnel. Genomic data may be retained for future reanalysis as scientific knowledge changes. Individual genetic variants may be submitted in de-identified form to public variant databases such as ClinVar; raw genomic data and medical records will not be included in those submissions.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Adults Undergoing Clinical Genome Sequencing | – | Genetic: Genome sequencingAdults with unexplained medical conditions or clinical presentations who undergo clinical genome sequencing and longitudinal follow-up |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- University of Washington - Montlake Campus or Harborview Medical Center Seattle, WA, USA
Key inclusion criteria (5 listed)
- Person has a medical condition that does not yet have a clear explanation
- Enough medical information is available within the UW Medicine system to evaluate the person's condition and interpret genetic test results
- A blood sample or cheek-swab sample can be collected for genetic testing
- The person does not already have a confirmed genetic diagnosis that fully explains their current medical condition
- The person, or their legally authorized representative when applicable, is willing and able to provide informed consent.
Key exclusion criteria (4 listed)
- The current illness has a clear non-genetic explanation, such as a traumatic injury, confirmed overdose or intoxication, or an infection that fully explains the illness
- The person previously had genetic testing specifically for the current condition or symptoms, including prior whole-exome or whole-genome sequencing
- The person is currently incarcerated.
- The person has had a donor stem cell, bone marrow transplant or active blood cancer that makes a sample unsuitable for testing their inherited genetic information
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 |
|---|---|---|
| Genome sequencingClinical whole-genome sequencing of blood or buccal DNA, with optional family comparator analysis and return of clinical results | Genetic | Adults Undergoing Clinical Genome Sequencing |
Primary outcome
Diagnostic Yield of Clinical Genome Sequencing
Time frame: Through study completion, an average of 3 years
Number and percentage of participants with one or more definitive or possible diagnostic findings on clinical genome sequencing. This will be further stratified as secondary outcome measures by clinical and demographic characteristics.
1 secondary outcome
Short-term and long-term changes in medical management
Time frame: At 6 months after testing and at 3 years after testing
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 22 Jul 2026.
- Public homepage for study details and updatesLink provided by the sponsor.
- Individual participant dataSharing planned: No. Individual participant data will not be made publicly available because the dataset includes sensitive clinical and genomic information. Aggregate study results may be shared through publications and presentations, and de-identified individual genetic variants may be submitted to public variant databases.
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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.
Evonne McArthur, MD, PhD principal investigator
University of Washington
Danny E Miller, MD, PhD study director
University of Washington
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hereditary Diseases and Critical Illness, run by University of Washington at 1 site in United States.
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 5 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: enrolling by invitation, as of the sponsor's last update on 22 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Diagnostic Yield of Clinical Genome Sequencing (time frame: Through study completion, an average of 3 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 22 Jul 2026.