PWS Outcomes Assessment Study

NCT04102839 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 59

Last updated 2024-11-04

No results posted yet for this study

Summary

This is a longitudinal study during which qualitative interviews will be conducted with caregivers of Soleno C601/C602 study subjects. There is an additional option for caregivers to collect video data of PWS patients doing specific activities of daily life.

The purpose of this study is to understand the real-world and nuanced impact of a potential therapeutic on individual PWS patients. The results of this study will complement the outcomes being captured during the Soleno C601/C602 clinical studies.

There is no treatment or intervention associated with this study.

Conditions

Interventions

OTHER

Interview

Qualitative Interview

Sponsors & Collaborators

  • Casimir Trials

    collaborator UNKNOWN
  • Soleno Therapeutics, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-15
Primary Completion
2021-06-08
Completion
2021-06-08

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04102839 on ClinicalTrials.gov