NCT06667583

Brief Summary

Our study aims to detect 5p15/ 9q22/ 15q22 hyperdiploidy and thier significance in Multiple Myeloma patients

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2024

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 29, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 31, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

December 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
Last Updated

November 1, 2024

Status Verified

October 1, 2024

Enrollment Period

1 year

First QC Date

October 29, 2024

Last Update Submit

October 30, 2024

Conditions

Keywords

Hyperdiploidy

Outcome Measures

Primary Outcomes (1)

  • detection of 5p15/ 9q22/ 15q22 hyperdiploidy and thier significance in Multiple Myeloma patients

    detection of 5p15/ 9q22/ 15q22 hyperdiploidy and thier significance in Multiple Myeloma patients

    up to 2 yeqrs

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Newly diagnosed Multiple Myeloma Patients

You may qualify if:

  • Newly diagnosed Multiple Myeloma Patients -

You may not qualify if:

  • Patient of Multiple Myeloma who received treatment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

Bone Marrow Aspirate

MeSH Terms

Conditions

Multiple MyelomaNeoplasms

Condition Hierarchy (Ancestors)

Neoplasms, Plasma CellNeoplasms by Histologic TypeHemostatic DisordersVascular DiseasesCardiovascular DiseasesParaproteinemiasBlood Protein DisordersHematologic DiseasesHemic and Lymphatic DiseasesHemorrhagic DisordersLymphoproliferative DisordersImmunoproliferative DisordersImmune System Diseases

Study Officials

  • dalia abd el naser, resident dr

    Assiut University

    PRINCIPAL INVESTIGATOR
  • Eman Zaki, Professor

    Assiut University

    STUDY DIRECTOR
  • safia hussein, Lecturer

    Assiut University

    STUDY DIRECTOR
  • mohammed El nagar, Ass profesor

    Assiut University

    STUDY DIRECTOR

Central Study Contacts

Dalia Abd el naser, resident dr

CONTACT

Safia Hussein, Lecturer

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
dr dalia gamal

Study Record Dates

First Submitted

October 29, 2024

First Posted

October 31, 2024

Study Start

December 1, 2024

Primary Completion

December 1, 2025

Study Completion

January 1, 2026

Last Updated

November 1, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will not share