Comparison of the Complications in Multiple Myeloma Patients Who Received Autologous Stem Cell Transplantation Between in HEPA-filtered Room and Non-HEPA-filtered Room

NCT ID: NCT06286241

Last Updated: 2024-03-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

344 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-03-25

Study Completion Date

2024-07-30

Brief Summary

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The goal of this observational study is to comparison of the complications in multiple myeloma patients who received autologous stem cell transplantation between in HEPA-filtered room and non-HEPA-filtered room. The main questions it aims to answer are:

* The incidence of febrile neutropenia, infection, and duration of hospital stay
* 2-year progression free survival Participants will be collected the data of baseline diagnosis, treatment, treatment results and complications during admission and follow-up visits from hospital medical record.

Detailed Description

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Conditions

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Multiple Myeloma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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HEPA-filtered room

multiple myeloma patients who received autologous stem cell transplantation were admitted in HEPA-filtered room

No interventions assigned to this group

non-HEPA-filtered room

multiple myeloma patients who received autologous stem cell transplantation were admitted in non-HEPA-filtered room

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* aged 18 - 65 years old
* Patients with multiple myeloma undergoing treatment with autologous stem cell transplantation and having a Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) score less than or equal to 2
* Patients must provide signed consent to participate in the research if they undergo ASCT after the study has been approved.
* If patients undergo ASCT before the study approval, retrospective data will be collected.

Exclusion Criteria

* Patients with concomitant other types of cancer
* Patients who refuse to participate in the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Siriraj Hospital

OTHER

Sponsor Role lead

Responsible Party

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Chutima Kunacheewa

lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Chutima Kunacheewa, MD

Role: CONTACT

+66896790959

Weerapat Owattanapanich, MD

Role: CONTACT

+66891081983

Other Identifiers

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877/2564(IRB2)

Identifier Type: -

Identifier Source: org_study_id

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