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Not yet recruitingNCT07911618Updated Nov 3, 2026

Data Collection For Patients With Sickle Cell Disease

An observational study in Data Collection and Sickle Cell Disease, sponsored by M.D. Anderson Cancer Center. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by M.D. Anderson Cancer Center · Observational

Updated Nov 3, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
500
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 733 studies in Anemia, Sickle Cell with a site in United States — 135 open to participants now, 186 under way, 16 of them phase 3. Anemia, Sickle Cell · United States.

Planned enrollment
28th of 168
500 · median 100
Started
2027
with 5 others
Observational
168 of 733
34 open now
Primary completion
2035-01
later than 169 of 182 live
Registered
733rd of 733
by date

Among the 733 studies in Anemia, Sickle Cell with a site in United States, this one is the 28th largest by planned enrollment of the 168 observational ones, is one of 6 that started in 2027, is one of 168 observational ones, reaches primary completion later than 169 of the 182 other live ones, and was the 733rd registered.

By phase

733 studies; the count open now beside each. This study's row is marked.

Observationalthis study168 · 34 open
No phase165 · 36 open
Phase 2161 · 23 open
Phase 198 · 13 open
Phase 1/260 · 13 open
Phase 350 · 10 open
Phase 420 · 4 open
Phase 2/37 · 1 open
Other kind4 · 1 open

By the year they started

First in 1984; this study’s year is marked. 6 started in 2027.

Size and results

Median enrollment 31 across the 559 interventional studies, 100 across the 168 observational. Of the 506 that completed or were terminated, 207 (41%) have results posted.

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Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 733 studies in Anemia, Sickle Cell with a site in United States, or all of them as a file.
02

Study summary

To create a database of clinical information, participant /disease characteristics, and treatment history collected from patients with Sickle Cell Disease.

Read the detailed description

Primary Objective To collect comprehensive data from patients who are being treated at UT Physicians and UT MDACC for sickle cell disease.

03

Conditions studied

  • Data Collection
  • Sickle Cell Disease

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04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

UT MD Anderson Cancer Center

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

  1. Participants 18 years of age and older diagnosed with Sickle Cell Disease.
  2. Participants treated at UT Physicians Sickle Center Cancer Center
  3. Participants treated at UT MD Anderson Cancer Center

Exclusion criteria

Exclusion Criteria None

05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
500 participants (estimated)
Patient registry
No

Interventions

  • Otherdata collection

    Data will be extracted from the electronic medical record system at UT Physicians and UT MDACC.

06

What researchers measure

Primary outcomes

  1. safety and adverse events (AEs)

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

    Time frame: Through study completion; an average of 1 year

07

Study locations

1 site
08

References and documents

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Apr 2027; primary completion for Jan 2035, 92 months later.

Of 130 non-industry observational studies under Anemia, Sickle Cell, half reached primary completion within 48 months of starting (the median), counting those still running; a quarter within 23 and three quarters within 109. This study's planned 92 months is above that.

Counting every sponsor, half of 139 studies reached it within 49 months; a quarter within 24 and three quarters within 109.

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

Registered
Oct 28, 2026
First posted
Nov 3, 2026
StartEst.
Apr 6, 2027
Primary completionEst.
Jan 1, 2035
CompletionEst.
Jan 1, 2037
Last update
Nov 3, 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.
Registered
First appeared on the registry. No changes since
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07911618
Responsible party
Sponsor
First posted
Nov 3, 2026
Start date
Apr 6, 2027 (estimated)
Primary completion
Jan 1, 2035 (estimated)
Completion
Jan 1, 2037 (estimated)
Last update
Nov 3, 2026

Study contacts

Partow Kebriaei, MD
Contact
pkebriae@mdanderson.org
713-745-0663
Partow Kebriaei, MD
principal investigator · UT MD Anderson Cancer Center

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 not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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