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.

Recruitment status

COMPLETED

Target enrollment

266890 participants

Primary outcome timeframe

A 20 year analysis period (1999-2018 inclusive)

Results posted on

2025-06-11

Participant Flow

Participant milestones

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

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

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

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

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

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

People With Ulcerative Colitis

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

People With Crohn's Disease

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

People With Psoriatic Arthritis

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

People With Rheumatoid Arthritis

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Maya H Buch

Centre for Musculoskeletal Research

Phone: +441613066000

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place