Chromosome Aberrations clinical trials
The registry lists 48 studies for Chromosome Aberrations across more than 10 countries. 10 are recruiting or about to start. 15 of them are mainly about Chromosome Aberrations (how this is decided). Per ClinicalTrials.gov, last updated 2026-11-10. Counting its 4 narrower conditions too, such as Aneuploidy: 192 studies, 36 open.
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Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
Now Active, not recruiting
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Who runs them
Igenomix (3) · Applied Spectral Imaging Ltd. (2) · Nanfang Hospital, Southern Medical University (2) · Assiut University (2) · National Human Genome Research Institute (NHGRI) (2) · Assisting Nature (2) · Gillette Children's Specialty Healthcare (1) · First Affiliated Hospital of Zhejiang University (1)
What is being tested here
Drugs under test in Chromosome Aberrations studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
The study
- Nov 2027MT2021-08T Cell Receptor Alpha/Beta Depletion PBSC Transplantation for Heme Malignancies · Masonic Cancer Center, University of Minnesota
Who these studies take
Of the 7 Chromosome Aberrations studies recruiting now, 4 (57%) set no upper age limit and 3 (43%) stop at 75 or younger. 3 (43%) take children under 18. 1 (14%) are for women only and 0 (0%) for men only; 4 (57%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 3 (43%) | 3 (43%) |
| 18 | 6 (86%) | 5 (71%) |
| 30 | 6 (86%) | 5 (71%) |
| 40 | 6 (86%) | 5 (71%) |
| 50 | 6 (86%) | 5 (71%) |
| 65 | 4 (57%) | 4 (57%) |
| 75 | 4 (57%) | 4 (57%) |
| 85 | 4 (57%) | 4 (57%) |
Across all 48 studies, recruiting or not: 56% stop at 75 or younger and 56% at 65; 46% take children; 29% are for women only and 2% for men only; 29% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
Studies
Recruiting first, then most recently updated. Showing 48 of 48. search them.
- Detection of Genetic Markers of Lung CancerRecruitingNCT002802021 country
- Biocollection in MyeloDysplastic Syndrome (P-MDS)RecruitingNCT04869683Not applicable1 country
- MT2021-08T Cell Receptor Alpha/Beta Depletion PBSC Transplantation for Heme MalignanciesRecruitingNCT05735717Phase 21 country
- Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal DisordersRecruitingNCT074930961 country
- Chromosome 18 Clinical Research CenterRecruitingNCT002272531 country
- Chromosomal Abnormalities in Patients With Congenital Heart Disease at Assiut University Children's HospitalNot yet recruitingNCT07204509
- Prevalence of Translocation Phenotyping in Children With Down Syndrome and Their ParentsNot yet recruitingNCT07175168
- Structural Chromosome Rearrangements and Brain DisordersEnrolling by invitationNCT060720791 country
- AnovaOS Network Powered Patient RegistryRecruitingNCT050139441 country
- The Relationship Between Fetal Membrane Thickness and Fetal Chromosomal AneuploidiesRecruitingNCT061412131 country
- Natural History Study of Smith-Magenis SyndromeCompletedNCT000135591 country
- Microarray Analysis in Syndromic ObesityCompletedNCT01043198Not applicable1 country
- Embryo Selection by Noninvasive Preimplantation Genetic TestCompletedNCT04339166Not applicable1 country
- RCT Study to Validate niPGT-A Clinical Benefit.TerminatedNCT04000152Not applicable5 countries
- North Carolina Genomic Evaluation by Next-generation Exome Sequencing, 2CompletedNCT03548779Not applicable1 country
- Technical Feasibility of the cfDNA Test for Non-invasive Cytogenetic Analysis of Early Miscarriages Versus the Gold Standard MicroarrayCompletedNCT059000761 country
- A Study of Chromosomal Abnormalities as a Predictor of Staging and Prognosis in Patients With Liver CancerActive, not recruitingNCT053718731 country
- Low-Dose Ketamine in Children With ADNP SyndromeCompletedNCT04388774Phase 1/21 country
- Multi-center Study to Validate niPGT-ACompletedNCT035209338 countries
- A Study of Selinexor in Combination With Daunorubicin and Cytarabine for Untreated AMLCompletedNCT02403310Phase 11 country
- Time Lapse Assisted Embryo Selection Versus Non Invasive PGT-A Assisted Embryo SelectionStatus unknownNCT055459951 country
- Invasive PGT-A Embryo Selection Versus Non Invasive PGT-A Assisted Embryo SelectionStatus unknownNCT055475551 country
- Influence of Molecular Abnormalities on Response of VAH vs. VEN+HMA in RR-AMLCompletedNCT054560481 country
- Utilizing Free DNA in Embryo Culture for PGTCompletedNCT02884063
- Post-operative Lite Run StudyCompletedNCT03135145Not applicable1 country
- Safety & Efficacy Study of Oral Panobinostat (LBH589) With Chemotherapy in Patients < 65 Years Old With Acute Myeloid Leukemia (AML)CompletedNCT01242774Phase 13 countries
- Clinical Value of Mosaicism Diagnosis on the Trophectoderm BiopsiesCompletedNCT036735921 country
- Validation of a NICS Method Using the Culture MediumCompletedNCT038792651 country
- Non-Invasive Chromosomal Evaluation of 22q11.2CompletedNCT025410581 country
- Genomic Instability in Vascular SurgeonsCompletedNCT043631901 country
- Risk-stratified Therapy Based on Molecular Cytogenetic Aberration and Treatment Response in AMLStatus unknownNCT036209551 country
- Application of UCAD for Diagnosing Urothelial Carcinoma.Status unknownNCT039983711 country
- Efficacy of Counseling for Prenatal Screening and Diagnostic Tests on Pregnant Women: Randomised Controlled StudyCompletedNCT03825978Not applicable1 country
- Prenatal Screening, Diagnosis and Intrauterine Intervention of Fetal Abnormal Chromosome and Structure in Twins PregnancyStatus unknownNCT02982356Not applicable
- Detection of Chromosomal Aberrations in Non-small Cell Lung Cancer (NSCLC) Using Fluorescent in Situ Hybridization (FISH) (ALK Test)CompletedNCT016208531 country
- Study on the Impact of Stem Cell Donation and Bone Marrow Harvesting on Unrelated DonorsCompletedNCT01884610
- Preimplantation Genetic Screening in Women of Advanced Maternal AgeCompletedNCT00795795Not applicable1 country
- Non-Invasive Screening for Fetal AneuploidyCompletedNCT008479901 country
- Effects of Methylphenidate on Cellular Abnormalities in Children With Attention Deficit Hyperactivity Disorder (ADHD)CompletedNCT00409708Phase 21 country
- Detection of Chromosomal Aberrations in Urine Samples Using Fluorescent in Situ Hybridization (FISH) (UroVysion Test)CompletedNCT012647441 country
- Preimplantation Genetic Diagnosis for the Indication of Advanced Reproductive AgeSuspendedNCT00646893Phase 42 countries
- How Dose Coenzyme Q10 Supplementation During Infertility Treatment Effects Pregnancy OutcomeTerminatedNCT00878124Not applicable1 country
- Chromosome Abnormalities in Chronic Myeloid Leukemia (CML) on Imatinib. GIST Patients on ImatinibTerminatedNCT00461929Phase 41 country
- Genetic Analysis of Fraser Syndrome and Fryns SyndromeCompletedNCT000328771 country
- Chromosomal Analysis of Single Cells in Human EmbryosStatus unknownNCT006143671 country
- Down Syndrome - Comparison of Screening Methods in the 1st and 2nd TrimestersStatus unknownNCT00006445Not applicable1 country
- Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion SyndromesCompletedNCT000043511 country
- Immunologic Evaluation in Patients With DiGeorge Syndrome or Velocardiofacial SyndromeStatus unknownNCT000051021 country