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Active, not recruitingNCT05149157SCRIPTUpdated Feb 19, 2025

Trajectories and Mechanisms of Recovery From Malaria: An Observational Study

An observational study in Malaria, sponsored by Imperial College London. Active, not recruiting at 1 site in United Kingdom. Open to participants aged 8 Days and older. Per ClinicalTrials.gov, last updated 2025-02-19.

Sponsored by Imperial College London · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2026, 9 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
240
Ages
8 Days and older
Sex
All
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Study summary

This observational research study aims to answer the question: 'Which aspects of human biology play an important role in recovery from symptomatic malaria?'

In particular, the researchers aim to identify human genes for which the level of gene activity reflects the patient's overall rate of recovery. The researchers believe this approach may reveal new targets for adjunctive therapies.

The researchers aim to recruit 240 people, of all ages, who have been diagnosed with symptomatic malaria at selected hospitals in London. Blood samples, urine samples, and clinical information will be collected over the 14 days following malaria diagnosis.

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Conditions studied

  • Malaria

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Keywords

  • Malaria
  • Recovery
  • Transcriptomics
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In context

Malaria

1,299 studies on the registry are indexed under Malaria; 86 are open to participants now.

This study's planned enrollment of 240 is below the median of 600 across 218 observational studies indexed under Malaria.

Browse Malaria studies →

Lead sponsor

Imperial College London is the lead sponsor of 824 studies on the registry; 178 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 6 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Days and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients of any age with symptomatic malaria confirmed by asexual stage parasitaemia (of any Plasmodium species) on blood film

Inclusion criteria

Patients of any age with symptomatic malaria confirmed by asexual stage parasitaemia (of any Plasmodium species) on blood film.

Exclusion criteria

Exclusion Criteria:

Patients with asymptomatic malaria; Patients with congenital malaria; Patients with Plasmodium gametocytaemia only; Patients with known HIV; Patients who have received antimalarial treatment for symptomatic malaria in the 28 days prior to hospital presentation; Patients who explicitly deny consent.

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
240 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Interventions

  • OtherSymptomatic malaria

    This observational study will be recruiting patients who have symptomatic malaria (confirmed by presence of asexual stage parasitaemia of any Plasmodium species on blood film)

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What researchers measure

Primary outcomes

  1. Genes for which expression (level of gene activity) correlates with a 'composite recovery score'

    The 'composite recovery score' will be calculated by principal component analysis of rates of recovery for individual markers of tissue, organ, or organ system dysfunction, and extraction of the value of the first principal component for each participant. Genes for which expression correlates with the 'composite recovery score' will be identified by whole blood transcriptome analysis.

    Time frame: Each study participant will be assessed over the 14 days following malaria diagnosis

Secondary outcomes

  1. Genes for which expression (level of gene activity) correlates with rate of recovery for individual markers of tissue, organ, or organ system dysfunction

    Genes for which expression correlates with the individual markers of tissue, organ, or organ system dysfunction will be identified by whole blood transcriptome analysis.

    Time frame: Each study participant will be assessed over the 14 days following malaria diagnosis

  2. Rate of recovery for individual markers of tissue, organ, or organ system dysfunction

    Rates of recovery will be calculated for individual markers of tissue, organ, or organ system dysfunction

    Time frame: Each study participant will be assessed over the 14 days following malaria diagnosis

  3. Sequences of clinical events predictive of recovery, as determined by Bayesian inference of dynamic pathways using the HyperTraPS statistical platform

    Hypercubic transition path sampling (HyperTraPS) will be used to characterise patterns of recovery and identify predictors of fast vs slow recovery

    Time frame: Each study participant will be assessed over the 14 days following malaria diagnosis

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Study locations

1 site
  • Imperial College Healthcare NHS Trust
    London, United Kingdom
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05149157
Lead sponsor
Imperial College London
Responsible party
Sponsor
First posted
Dec 8, 2021
Start date
Aug 2, 2022
Primary completion
Jan 5, 2026 (estimated)
Completion
Jan 5, 2026 (estimated)
Last update
Feb 19, 2025

Study contacts

Aubrey Cunnington, PhD
principal investigator · Imperial College London

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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