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Recruiting NCT06377059

NCT06377059 Early Detection of Complications During Immunotherapy for Haematological Malignancy

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Clinical Trial Summary
NCT ID NCT06377059
Status Recruiting
Phase
Sponsor Rigshospitalet, Denmark
Condition Hematologic Cancer
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2024-12-02
Primary Completion 2026-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
WARD

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2024-12-02 with a primary completion date of 2026-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Aims * To identify patients that should remain admitted in hospital for more intense surveillance because of high risk for development of clinical complications * Expand the understanding of the interactions between physiology and immunology for the design of future projects and general knowledge Hypothesis Development of a risk model based on a combination of physiological and immunological parameters can contribute to early detection of patients at risk for clinical complications after anti-cancer treatment.

Eligibility Criteria

Inclusion Criteria: * Age ≥ 18 years * Patients diagnosed with haematologic malignant disease (e.g. malignant lymphoma) * Patients scheduled for treatment with CART or BsAbs Exclusion Criteria: * Patient is pregnant * Patient has a pacemaker * Patient is allergic to one or more of the materials that the equipment consists of * Investigator deems patient not able to comply with participation in the study

Contact & Investigator

Central Contact

Sandra Egedie Lyby Taylor Pitter, MD

✉ sandra.egedie.taylor.pitter@regionh.dk

📞 +4540309153

Principal Investigator

Sandra Egedie Lyby Taylor Pitter, MD

PRINCIPAL INVESTIGATOR

Rigshospitalet, Denmark

Frequently Asked Questions

Who can join the NCT06377059 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Hematologic Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06377059 currently recruiting?

Yes, NCT06377059 is actively recruiting participants. Contact the research team at sandra.egedie.taylor.pitter@regionh.dk for enrollment information.

Where is the NCT06377059 trial being conducted?

This trial is being conducted at Copenhagen O, Denmark.

Who is sponsoring the NCT06377059 clinical trial?

NCT06377059 is sponsored by Rigshospitalet, Denmark. The principal investigator is Sandra Egedie Lyby Taylor Pitter, MD at Rigshospitalet, Denmark. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology