Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Clinical Procedures to Support Research in ALS

Key facts

Where
Durham, Irvine, Kansas City, Miami, Minneapolis, New York, Palo Alto, Portland, San Antonio, San Francisco, and Winston-Salem, United StatesSee the 11 sites

Where in United States

  • Duke UniversityDurham, United StatesTaking people
  • University of California, IrvineIrvine, United StatesTaking people
  • University of Kansas Medical CenterKansas City, United StatesTaking people
  • University of MiamiMiami, United StatesTaking people
  • Hennepin County Medical CenterMinneapolis, United StatesTaking people
  • Columbia UniversityNew York, United StatesNo longer taking part
  • Stanford UniversityPalo Alto, United StatesTaking people
  • Providence Health & ServicesPortland, United StatesTaking people
  • University of Texas - San Antonio - Health Science CenterSan Antonio, United StatesTaking people
  • California Pacific Medical CenterSan Francisco, United StatesTaking people
  • Wake Forest UniversityWinston-Salem, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Miami
Trial code
NCT03489278
Record updated
15 June 2026
Original description
The purpose of the Clinical Procedures To Support Research (CAPTURE) study is to utilize information collected in the medical record to learn more about a disease called amyotrophic lateral sclerosis (ALS) and related disorders.Read full original descriptionShow less

Clinical Procedures to Support Research in ALS (CAPTURE-ALS)

The purpose of the Clinical Procedures To Support Research (CAPTURE) study is to utilize information collected in the medical record to learn more about a disease called amyotrophic lateral sclerosis (ALS) and related disorders.

Inclusion: Diagnosis of ALS or a related disorder (e.g. primary lateral sclerosis, progressive muscular atrophy); Receiving care at a clinical center that uses Epic as its EHR; Able and willing to provide informed consent (or informed consent obtainable from a designated proxy).

Exclusion: Inability to understand English and/or Spanish.

ClinicalTrials.gov NCT03489278