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Active, not recruitingNCT03473795Updated Aug 18, 2026

Developing Non-Communicable Disease Registries in Africa : A Step Towards Providing Quality Data for Improving Patient Outcomes

An observational study in Non-Communicable Disease, sponsored by Memorial Sloan Kettering Cancer Center. Active, not recruiting at 14 sites in 2 countries. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-18.

Sponsored by Memorial Sloan Kettering Cancer Center · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
6,990
Ages
18 Years and older
Sex
All
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Study summary

This umbrella protocol seeks to develop robust data registries for non-communicable diseases (NCDs) in sub-Saharan Africa (SSA) with the aim of providing accurate and comprehensive data for the evaluation of such diseases in sub-Saharan African countries.Healthy volunteers will be included in the study for comparison.

Additionally, the investigators aim to describe the gut microbiome community diversity of a cohort of community dwelling Nigerians and compare with CRC patients in Nigerian and at MSK. We will collect stool for microbiome and metabolomic analysis from community dwelling persons in the catchment area of ARGO facilities in Nigeria while contemporaneously administering an extensive medical and environmental exposure questionnaire.

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Conditions studied

  • Non-Communicable Disease

Keywords

  • Patient Outcomes
  • 18-114
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In context

Noncommunicable Diseases

144 studies on the registry are indexed under Noncommunicable Diseases; 55 are open to participants now.

This study's enrollment of 6,990 is above the median of 1,674 across 48 observational studies indexed under Noncommunicable Diseases.

Browse Noncommunicable Diseases studies →

Lead sponsor

Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,964 studies on the registry; 327 are open to participants now.

Of its 135 completed or terminated interventional studies of FDA-regulated products, 71 (53%) have results posted.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will be accrued in medical clinics in Africa as determined by the local investigators and local research staff.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 and older.
  • Suspected or confirmed diagnosis of a non-communicable disease. OR
  • Healthy volunteers/no confirmed diagnosis for comparison.

Exclusion criteria

Exclusion Criteria:

  • Participants unwilling to sign consent.
  • Participants under the age of 18
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Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
6,990 participants (actual)
Target follow-up
5 Years
Patient registry
Yes
Biospecimen retention
Samples with dna

Groups and cohorts

  • healthy participants and participants diagnosed with NCDs

    This protocol will entail prospective collection of data on healthy participants and participants diagnosed with NCDs managed at collaborating institutions in SSA. Information to be obtained includes socio-demographic data, risk factors, disease-specific data, investigation and treatment details, as well as findings during follow-up. Particular reference will be made to outcome measures such as local and distant recurrence, survival and mortality. Follow-up data will be updated during clinic visits and also via phone calls.

    Behavioral: Questionnaire forms · Other: Bio-specimen samples

Interventions

  • BehavioralQuestionnaire forms

    The questionnaires will include information such as socio-demographic data, risk factors, disease specific data, investigation and treatment details as well as findings during followup. Particular reference will be made to outcome measures such as local and distant recurrence, survival and mortality.

  • OtherBio-specimen samples

    Samples can include tissue, blood, urine, saliva, hair and nail clipping.

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What researchers measure

Primary outcomes

  1. # of patients that develope non-communicable diseases in Africa

    Time frame: 5 years

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Study locations

14 sites
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References and documents

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2018 (actual). Primary completion is estimated for Mar 2027, 108 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 16, 2018
First posted
Mar 22, 2018
StartActual
Mar 16, 2018
Primary completionEst.
Mar 2027
CompletionEst.
Mar 2027
Last update
Aug 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 18, 2026, 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
NCT03473795
Responsible party
Sponsor
First posted
Mar 22, 2018
Start date
Mar 16, 2018
Primary completion
Mar 2027 (estimated)
Completion
Mar 2027 (estimated)
Last update
Aug 18, 2026

Study contacts

T. Peter Kingham, MD
principal investigator · Memorial Sloan Kettering Cancer Center

Oversight

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 Aug 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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