Oncology Clinical Trial
Official title:
CCG-LTFI: A Groupwide Protocol for Collecting Follow- up Data
This protocol is not an independent research study, but rather a means to aggregate Children's Cancer Group protocols that are closed to patient entry for the purpose of collecting current status information on those patients treated under those protocols.
Children's Cancer Group clinical trials are conducted to improve understanding of the
biology and treatment of childhood cancers. Protocols are developed by expert committees and
distributed from the Group Operations Center to the member institutions. Before a protocol
can be opened to patient accrual at a CCG institution, the protocol, consent form and any
activation amendments are reviewed and approved by the local Institutional Review Board
QRB).
Protocols remain open to patient accrual until sufficient evaluable patients have been
entered to answer the study questions. During this time, the protocol and any new amendments
are reviewed annually by the IRB. When the study has been closed to patient accrual it
remains open solely for the purpose of collecting life status and occurrence of adverse
events. The IRB must continue its annual review as long as a patient treated on the protocol
is alive and follow-up data are being collected. The CCG Long Term Follow-up protocol
(CCG-LTF1) is meant to allow continued collective review of all protocols that meet the
following criteria: (a) It is closed to patient accrual, (b) all patients have completed
treatment, and (c) there are patients who are alive and being followed. The protocols that
meet these criteria will be listed as being aggregated under CCG-LTF1 such that an IRB
review of CCG-LTF1 will constitute a review of that protocol.
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Time Perspective: Prospective
Status | Clinical Trial | Phase | |
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Completed |
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Phase 1 | |
Recruiting |
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Exactech Humeral Reconstruction Prosthesis of Shoulder Arthroplasty PMCF (HRP)
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||
Active, not recruiting |
NCT06015009 -
Symptom Management App for Children at the Early Stage of Cancer Survivorship and Their Caregivers
|
N/A | |
Active, not recruiting |
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Risk Scoring Model for Endometrial Cancer
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||
Recruiting |
NCT05055609 -
Open-Label, Dose-Escalation With Expansion to Assess the Safety, Tolerability, and PK of TRE-515 in Subjects With Solid Tumors
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Phase 1 | |
Not yet recruiting |
NCT04324320 -
Psychological Distress in Outpatient Oncological Rehabilitation
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||
Recruiting |
NCT06222801 -
The 1st Tumor CytokinoTherapy Database (TCTD-1)
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||
Recruiting |
NCT03831633 -
Comparative Effectiveness of AKYNZEO® and Standard of Care (Including EMEND®) for the Prevention of Nausea and Vomiting (CINV) in Cancer Patients
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Phase 4 | |
Completed |
NCT04914702 -
Feasibility and Comparison of Continuously Monitored Vital Signs in Pediatric Patients With Cancer.
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||
Recruiting |
NCT05198570 -
Pharmacokinetics of Intravenous Acyclovir in Oncologic Paediatric Patients
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Recruiting |
NCT05712174 -
A Study of [18]F-PSMA-1007 in Patients With Known or Suspected Metastatic Prostate Cancer
|
Phase 2 | |
Recruiting |
NCT03832062 -
Value of Analysing Under-utilised Leftover Tissue (VauLT)
|
||
Completed |
NCT03988777 -
Magnetic Seed Localisation for Nonpalpable Breast Lesions
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||
Recruiting |
NCT06031233 -
Evaluating the Safety of Shortened Infusion Times for dIfferent Oncological Immunotherapie
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Phase 4 | |
Enrolling by invitation |
NCT04019119 -
Digital Intervention for the Modification of Lifestyles (iGame)
|
N/A | |
Not yet recruiting |
NCT05926362 -
Capillary-Venous Paired Data Collection
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||
Recruiting |
NCT05686213 -
ExeNTrO: Exercise During Neoadjuvant Chemoradiation Treatment to Improve Rectal and Esophageal Cancer Outcome - Pilot Trial
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Phase 2 | |
Recruiting |
NCT05510856 -
Comparative Clinical Study Evaluating the Possible Efficacy of Duloxetine, Gabapentin and Lacosamide on Oxaliplatin-Induced Peripheral Neuropathy in Cancer Patients
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Phase 4 | |
Completed |
NCT04180306 -
PEWS Implementation in an LMIC Setting
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N/A | |
Completed |
NCT04933604 -
LPN in Patients With High-complex Renal Tumors
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