Trial Outcomes & Findings for The Risk of Venous Thromboembolism in Systemic Inflammatory Disorders: a United Kingdom (UK) Matched Cohort Study (NCT NCT03835780)
NCT ID: NCT03835780
Last Updated: 2025-06-11
Results Overview
Number of participants with systemic inflammatory disorders developing VTE (a composite of pulmonary embolism (PE) and deep vein thrombosis (DVT)) compared to population controls.
COMPLETED
266890 participants
A 20 year analysis period (1999-2018 inclusive)
2025-06-11
Participant Flow
Participant milestones
| Measure |
Controls
Age, gender and primary care practice matched individuals without an existing or incident diagnosis of IBD, RA, or PsA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Ulcerative Colitis
All individuals with an existing or incident diagnosis of ulcerative colitis during the study period
No intervention: A observation of outcomes in usual practice
|
People With Crohn's Disease
All individuals with an existing or incident diagnosis of Crohn's during the study period
No intervention: A observation of outcomes in usual practice
|
People With Psoriatic Arthritis
All individuals with an existing or incident diagnosis of IBD during the study period
No intervention: A observation of outcomes in usual practice
|
People With Rheumatoid Arthritis
All individuals with an existing or incident diagnosis of RA during the study period
No intervention: A observation of outcomes in usual practice
|
|---|---|---|---|---|---|
|
Overall Study
STARTED
|
213512
|
14182
|
9489
|
6297
|
23410
|
|
Overall Study
COMPLETED
|
213512
|
14182
|
9489
|
6297
|
23410
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
The Risk of Venous Thromboembolism in Systemic Inflammatory Disorders: a United Kingdom (UK) Matched Cohort Study
Baseline characteristics by cohort
| Measure |
Controls
n=213512 Participants
Age, gender and primary care practice matched individuals without an existing or incident diagnosis of IBD, RA, or PsA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Ulcerative Colitis
n=14182 Participants
All individuals with an existing or incident diagnosis of ulcerative colitis during the study period
No intervention: A observation of outcomes in usual practice
|
People With Crohn's Disease
n=9489 Participants
All individuals with an existing or incident diagnosis of Crohn's disease during the study period
No intervention: A observation of outcomes in usual practice
|
People With Psoriatic Arthritis
n=6297 Participants
All individuals with an existing or incident diagnosis of IBD during the study period
No intervention: A observation of outcomes in usual practice
|
People With Rheumatoid Arthritis
n=23410 Participants
All individuals with an existing or incident diagnosis of RA during the study period
No intervention: A observation of outcomes in usual practice
|
Total
n=266890 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|---|
|
Age, Continuous
|
51.7 years
STANDARD_DEVIATION 17.8 • n=5 Participants
|
47.2 years
STANDARD_DEVIATION 17.0 • n=7 Participants
|
41.8 years
STANDARD_DEVIATION 16.6 • n=5 Participants
|
49.2 years
STANDARD_DEVIATION 13.8 • n=4 Participants
|
59.0 years
STANDARD_DEVIATION 15.5 • n=21 Participants
|
49.8 years
STANDARD_DEVIATION 6.3 • n=8 Participants
|
|
Sex: Female, Male
Female
|
128129 Participants
n=5 Participants
|
7056 Participants
n=7 Participants
|
5193 Participants
n=5 Participants
|
3204 Participants
n=4 Participants
|
16634 Participants
n=21 Participants
|
160216 Participants
n=8 Participants
|
|
Sex: Female, Male
Male
|
85383 Participants
n=5 Participants
|
7126 Participants
n=7 Participants
|
4296 Participants
n=5 Participants
|
3093 Participants
n=4 Participants
|
6776 Participants
n=21 Participants
|
106674 Participants
n=8 Participants
|
|
Race/Ethnicity, Customized
Asian
|
9569 Participants
n=5 Participants
|
724 Participants
n=7 Participants
|
347 Participants
n=5 Participants
|
249 Participants
n=4 Participants
|
1114 Participants
n=21 Participants
|
12003 Participants
n=8 Participants
|
|
Race/Ethnicity, Customized
Black
|
4121 Participants
n=5 Participants
|
127 Participants
n=7 Participants
|
91 Participants
n=5 Participants
|
22 Participants
n=4 Participants
|
403 Participants
n=21 Participants
|
4764 Participants
n=8 Participants
|
|
Race/Ethnicity, Customized
Mixed
|
1483 Participants
n=5 Participants
|
85 Participants
n=7 Participants
|
67 Participants
n=5 Participants
|
44 Participants
n=4 Participants
|
150 Participants
n=21 Participants
|
1829 Participants
n=8 Participants
|
|
Race/Ethnicity, Customized
Other
|
1448 Participants
n=5 Participants
|
93 Participants
n=7 Participants
|
54 Participants
n=5 Participants
|
26 Participants
n=4 Participants
|
123 Participants
n=21 Participants
|
1744 Participants
n=8 Participants
|
|
Race/Ethnicity, Customized
White
|
148832 Participants
n=5 Participants
|
10099 Participants
n=7 Participants
|
6763 Participants
n=5 Participants
|
4727 Participants
n=4 Participants
|
17119 Participants
n=21 Participants
|
187540 Participants
n=8 Participants
|
|
Race/Ethnicity, Customized
Missing
|
48059 Participants
n=5 Participants
|
3054 Participants
n=7 Participants
|
2167 Participants
n=5 Participants
|
1229 Participants
n=4 Participants
|
4501 Participants
n=21 Participants
|
59010 Participants
n=8 Participants
|
|
Body mass index
Underweight (BMI ≤18.5)
|
4704 Participants
n=5 Participants
|
368 Participants
n=7 Participants
|
536 Participants
n=5 Participants
|
60 Participants
n=4 Participants
|
607 Participants
n=21 Participants
|
6275 Participants
n=8 Participants
|
|
Body mass index
Normal weight (BMI 18.5-25)
|
73675 Participants
n=5 Participants
|
5721 Participants
n=7 Participants
|
4225 Participants
n=5 Participants
|
1576 Participants
n=4 Participants
|
7758 Participants
n=21 Participants
|
92955 Participants
n=8 Participants
|
|
Body mass index
Overweight (BMI 25-30)
|
67076 Participants
n=5 Participants
|
4352 Participants
n=7 Participants
|
2446 Participants
n=5 Participants
|
2131 Participants
n=4 Participants
|
7735 Participants
n=21 Participants
|
83740 Participants
n=8 Participants
|
|
Body mass index
Obese (BMI ≥30)
|
44303 Participants
n=5 Participants
|
2367 Participants
n=7 Participants
|
1386 Participants
n=5 Participants
|
2071 Participants
n=4 Participants
|
5787 Participants
n=21 Participants
|
55914 Participants
n=8 Participants
|
|
Body mass index
BMI not recorded
|
23754 Participants
n=5 Participants
|
1374 Participants
n=7 Participants
|
896 Participants
n=5 Participants
|
459 Participants
n=4 Participants
|
1523 Participants
n=21 Participants
|
28006 Participants
n=8 Participants
|
|
Smoking status
Non-Smoker
|
94985 Participants
n=5 Participants
|
6328 Participants
n=7 Participants
|
3917 Participants
n=5 Participants
|
2522 Participants
n=4 Participants
|
8853 Participants
n=21 Participants
|
116605 Participants
n=8 Participants
|
|
Smoking status
Current Smoker
|
52035 Participants
n=5 Participants
|
2574 Participants
n=7 Participants
|
2914 Participants
n=5 Participants
|
1519 Participants
n=4 Participants
|
6063 Participants
n=21 Participants
|
65105 Participants
n=8 Participants
|
|
Smoking status
Ex-Smoker
|
63798 Participants
n=5 Participants
|
5147 Participants
n=7 Participants
|
2551 Participants
n=5 Participants
|
2232 Participants
n=4 Participants
|
8385 Participants
n=21 Participants
|
82113 Participants
n=8 Participants
|
|
Smoking status
Smoking status not recorded
|
2694 Participants
n=5 Participants
|
133 Participants
n=7 Participants
|
107 Participants
n=5 Participants
|
24 Participants
n=4 Participants
|
109 Participants
n=21 Participants
|
3067 Participants
n=8 Participants
|
|
Alcohol intake
Non-drinker
|
36623 Participants
n=5 Participants
|
2371 Participants
n=7 Participants
|
1798 Participants
n=5 Participants
|
1035 Participants
n=4 Participants
|
5404 Participants
n=21 Participants
|
47231 Participants
n=8 Participants
|
|
Alcohol intake
Within limits
|
117939 Participants
n=5 Participants
|
7727 Participants
n=7 Participants
|
4917 Participants
n=5 Participants
|
3508 Participants
n=4 Participants
|
13164 Participants
n=21 Participants
|
147255 Participants
n=8 Participants
|
|
Alcohol intake
Over recommended limits
|
30096 Participants
n=5 Participants
|
2083 Participants
n=7 Participants
|
1228 Participants
n=5 Participants
|
1067 Participants
n=4 Participants
|
2767 Participants
n=21 Participants
|
37241 Participants
n=8 Participants
|
|
Alcohol intake
Alcoholism
|
3438 Participants
n=5 Participants
|
217 Participants
n=7 Participants
|
138 Participants
n=5 Participants
|
128 Participants
n=4 Participants
|
340 Participants
n=21 Participants
|
4261 Participants
n=8 Participants
|
|
Alcohol intake
Alcohol level not recorded
|
25416 Participants
n=5 Participants
|
1784 Participants
n=7 Participants
|
1408 Participants
n=5 Participants
|
559 Participants
n=4 Participants
|
1735 Participants
n=21 Participants
|
30902 Participants
n=8 Participants
|
|
Index of multiple deprivation (IMD) quintile
1 (most deprived)
|
29144 Participants
n=5 Participants
|
1689 Participants
n=7 Participants
|
1324 Participants
n=5 Participants
|
803 Participants
n=4 Participants
|
3477 Participants
n=21 Participants
|
36437 Participants
n=8 Participants
|
|
Index of multiple deprivation (IMD) quintile
2
|
32323 Participants
n=5 Participants
|
2109 Participants
n=7 Participants
|
1518 Participants
n=5 Participants
|
919 Participants
n=4 Participants
|
3728 Participants
n=21 Participants
|
40597 Participants
n=8 Participants
|
|
Index of multiple deprivation (IMD) quintile
3
|
41379 Participants
n=5 Participants
|
2680 Participants
n=7 Participants
|
1901 Participants
n=5 Participants
|
1250 Participants
n=4 Participants
|
4739 Participants
n=21 Participants
|
51949 Participants
n=8 Participants
|
|
Index of multiple deprivation (IMD) quintile
4
|
50087 Participants
n=5 Participants
|
3475 Participants
n=7 Participants
|
2186 Participants
n=5 Participants
|
1452 Participants
n=4 Participants
|
5326 Participants
n=21 Participants
|
62526 Participants
n=8 Participants
|
|
Index of multiple deprivation (IMD) quintile
5 (least deprived)
|
56209 Participants
n=5 Participants
|
3963 Participants
n=7 Participants
|
2350 Participants
n=5 Participants
|
1720 Participants
n=4 Participants
|
5651 Participants
n=21 Participants
|
69893 Participants
n=8 Participants
|
|
Index of multiple deprivation (IMD) quintile
IMD not recorded
|
4370 Participants
n=5 Participants
|
266 Participants
n=7 Participants
|
210 Participants
n=5 Participants
|
153 Participants
n=4 Participants
|
489 Participants
n=21 Participants
|
5488 Participants
n=8 Participants
|
PRIMARY outcome
Timeframe: A 20 year analysis period (1999-2018 inclusive)Number of participants with systemic inflammatory disorders developing VTE (a composite of pulmonary embolism (PE) and deep vein thrombosis (DVT)) compared to population controls.
Outcome measures
| Measure |
People With Ulcerative Colitis (UC)
n=14182 Participants
All individuals with an existing or incident diagnosis of UC during the study period
No intervention: A observation of outcomes in usual practice
|
People With Rheumatoid Arthritis
n=23410 Participants
All individuals with an existing or incident diagnosis of RA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Psoriatic Arthritis
n=6297 Participants
All individuals with an existing or incident diagnosis of IBD during the study period
No intervention: A observation of outcomes in usual practice
|
Controls
n=213512 Participants
Age, gender and primary care practice matched individuals without an existing or incident diagnosis of IBD, RA, or PsA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Crohn's Disease
n=9489 Participants
All individuals with an existing or incident diagnosis of Crohn's disease during hte study period
|
|---|---|---|---|---|---|
|
Risk of Venous Thromboembolism (VTE)
|
335 Participants
|
845 Participants
|
132 Participants
|
3804 Participants
|
220 Participants
|
SECONDARY outcome
Timeframe: A 20 year analysis period (1999-2018 inclusive)Number of participants with systemic inflammatory disorders developing PE compared to population controls.
Outcome measures
| Measure |
People With Ulcerative Colitis (UC)
n=14182 Participants
All individuals with an existing or incident diagnosis of UC during the study period
No intervention: A observation of outcomes in usual practice
|
People With Rheumatoid Arthritis
n=23408 Participants
All individuals with an existing or incident diagnosis of RA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Psoriatic Arthritis
n=6297 Participants
All individuals with an existing or incident diagnosis of IBD during the study period
No intervention: A observation of outcomes in usual practice
|
Controls
n=213509 Participants
Age, gender and primary care practice matched individuals without an existing or incident diagnosis of IBD, RA, or PsA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Crohn's Disease
n=9489 Participants
All individuals with an existing or incident diagnosis of Crohn's disease during hte study period
|
|---|---|---|---|---|---|
|
Risk of Pulmonary Embolism (PE)
|
149 Participants
|
373 Participants
|
52 Participants
|
1737 Participants
|
98 Participants
|
SECONDARY outcome
Timeframe: A 20 year analysis period (1999-2018 inclusive)Number of participants with systemic inflammatory disorders developing DVT compared to population controls.
Outcome measures
| Measure |
People With Ulcerative Colitis (UC)
n=14182 Participants
All individuals with an existing or incident diagnosis of UC during the study period
No intervention: A observation of outcomes in usual practice
|
People With Rheumatoid Arthritis
n=23408 Participants
All individuals with an existing or incident diagnosis of RA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Psoriatic Arthritis
n=6297 Participants
All individuals with an existing or incident diagnosis of IBD during the study period
No intervention: A observation of outcomes in usual practice
|
Controls
n=213510 Participants
Age, gender and primary care practice matched individuals without an existing or incident diagnosis of IBD, RA, or PsA during the study period
No intervention: A observation of outcomes in usual practice
|
People With Crohn's Disease
n=9489 Participants
All individuals with an existing or incident diagnosis of Crohn's disease during hte study period
|
|---|---|---|---|---|---|
|
Risk of Deep Vein Thrombosis (DVT)
|
207 Participants
|
542 Participants
|
89 Participants
|
2335 Participants
|
140 Participants
|
Adverse Events
Controls
People With Ulcerative Colitis
People With Crohn's Disease
People With Psoriatic Arthritis
People With Rheumatoid Arthritis
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place