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NCT06608719Completed

Retrospective Study on the Safety and Therapeutic/Improvement Effects of Intravenous Administration of SHED-CM for ALS (SHED-CAH2023)

Retrospective Study on the Safety and Therapeutic/Improvement Effects of Intravenous Administration of SHED-CM for ALS

Source: ClinicalTrials.gov · Last updated 23 Sept 2024

Brief summary (registry, in English)

In this study, we will retrospectively evaluate the safety and efficacy of administering SHED-CM for the treatment of ALS.

Status (registry)
Completed
Study type
Observational
Enrollment
24 (actual)
First submitted
18 Jul 2024
Start date
25 Dec 2023
Primary completion date
1 Jul 2024
Lead sponsor
Hitonowa Medical
NCT number
NCT06608719

What you commit to

  • Study type: Observational
  • Participants enrolled: 24
  • From 25 Dec 2023 to the primary completion date, 1 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients who have a tracheostomy at the time of visit.
  • Patients who have expressed their refusal to participate in this study.

Who the study is looking for

  • patients who visited our clinic between January 1, 2022 and November 30, 2023 and have been diagnosed with ALS
  • male and female patients aged between 16 and 90 years old
  • ALSFRS-R score of 12 or more at the time of initial visit

Age in the registry: 38 years to 81 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hitonowa Medical
Coordinator of this site? Confirm its status
Chiyoda CityJapanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.