Evidence map›Paper›PMID 39622566›Full record

ArticleBMJ open2024

Phase I/II trial of intracerebral transplantation of autologous bone marrow stem cells combined with recombinant peptide scaffold for patients with chronic intracerebral haemorrhage: a study protocol.

Masahito Kawabori, Hideo Shichinohe, Kaoru Kahata, Arisa Miura, Kenichiro Maeda, Yoichi M Ito, Masahiko Mukaino, Ryo Kogawa, Kentaro Nakamura, Shuho Gotoh and 2 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Masahito KawaboriDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan masahitokawabori@yahoo.co.jp.ORCID http://orcid.org/0000-0002-3574-8380
Hideo ShichinoheInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, Japan.
Kaoru KahataInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, Japan.
Arisa MiuraInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, Japan.
Kenichiro MaedaInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, Japan.
Yoichi M ItoInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, Japan.
Masahiko MukainoDepartment of Rehabilitation, Hokkaido University Hospital, Sapporo, Japan.
Ryo KogawaBioscience & Engineering Laboratory, FUJIFILM Corporation, Ashigarakamigun, Japan.
Kentaro NakamuraBioscience & Engineering Laboratory, FUJIFILM Corporation, Ashigarakamigun, Japan.
Shuho GotohDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Kota KurisuDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Miki FujimuraDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIntracerebral haemorrhage (ICH) stands as a leading global cause of death and disability, posing a significant challenge with limited treatment options, especially for chronic patients. Recent advances in stem cell therapies have opened new avenues for therapeutic potential. Our previous preclinical research has demonstrated that intracerebral transplantation of bone marrow stromal cells (BMSCs) combined with a recombinant human collagen type I scaffold enables higher cell survival and engraftment and holds promising potential. In this article, we present the protocol for a novel clinical trial, named 'Research on Advanced Intervention using Novel Bone MarrOW stem cells for chronic intracerebral haemorrhage' (RAINBOW-Hx). METHODS AND ANALYSIS: RAINBOW-Hx is a phase I/II, open-label, uncontrolled study with the primary objective of assessing the safety and efficacy of intracerebral transplantation of autologous BMSCs combined with the scaffold (HUFF-01) in patients with chronic ICH. Eight patients, experiencing moderate to severe neurological deficits for 12 months or longer, will be enrolled. The haemorrhage location will be limited to the basal ganglia and thalamus. Approximately 50 mL of bone marrow will be extracted from the iliac bone of each patient, and BMSCs will be cultured using autologous platelet lysate. 3 days before transplantation, BMSCs will be combined with the scaffold to generate HUFF-01. Each patient will receive a 50 000 HUFF-01 dose, containing approximately 50 million BMSCs, through stereotactic transplantation into the haemorrhagic cavity. Neurological assessments, MRI, ETHICS AND DISSEMINATION: The trial protocols were reviewed and approved by the Institutional Review Board of the Hokkaido University Hospital (R5-11), and this study is conducted according to Good Clinical Practice guidelines and the principles of the Declaration of Helsinki. The results of this trial will be submitted for publication in a peer-reviewed scientific journal. TRIAL REGISTRATION NUMBER: jRCT2013230053, Japan Registry of Clinical Trials.

Indexed as

Cerebral HemorrhageAdultChronic DiseaseClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicFemaleHumansMaleMesenchymal Stem Cell TransplantationMiddle AgedTissue ScaffoldsTransplantation, AutologousClinical trialsIntracerebral HaemorrhageStroke Medicine

Identifiers

PMID39622566
PMCPMC11624737

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.