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Research for Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue (CFS/ME)

Study acronym: IMPROFA
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated May 29, 2025 (before its estimated July 1, 2025 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Lead sponsor: University Hospital, Saarland to Universität des Saarlandes
    • Primary completion date: Nov 1, 2024 to Jul 1, 2025
    • Study completion date: Dec 1, 2024 to Dec 1, 2025
    v7
  2. Primary completion date: Nov 1, 2022 to Nov 1, 2024
    • Study completion date: Dec 1, 2022 to Dec 1, 2024
    v6
  3. Re-verified, no change to tracked fieldsv5
  4. Primary completion date: Dec 1, 2020 to Nov 1, 2022
    • Start date: Aug 20, 2019 to Jul 20, 2021
    • Study completion date: Dec 1, 2021 to Dec 1, 2022
    v4
  5. Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Apr 1, 2020 to Dec 1, 2020
    • Start date changed from estimate of Apr 1, 2019 to Aug 20, 2019
    • Study sites: 0 to 1
    • Study completion date: Apr 1, 2021 to Dec 1, 2021
  6. Study description expanded, about 2 wordsv2
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Research for Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue Syndrome (CFS/ME) by Lipidomics, Metabolomics, Intestinal and Peritoneal Microbiome Analysis and Exome Analysis and Investigation of a Possible Benefit of Probiotics.
Trial Details
NCT Number NCT03773003
Lead Sponsor Universität des Saarlandes
Conditions
(from sponsor)		 Cancer Related Fatigue, Fatigue Syndrome, Chronic
Related terms Fatigue Syndrome, Chronic
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov