A Multi-Center Trial to Compare Three Doses of Meloxicam and Placebo in Patients With Rheumatoid Arthritis

Sponsor
Boehringer Ingelheim (Industry)
Overall Status
Completed
CT.gov ID
NCT00042068
Collaborator
(none)
1,000
153
13
6.5
0.5

Study Details

Study Description

Brief Summary

A 12-week trial consisting of 5 visits (6 if follow up is needed) to find out how effective and safe three different doses of meloxicam are compared with placebo in Rheumatoid Arthritis. Patient will take one dose of study medication daily.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double
Official Title:
A Multi-center, Double-Blind, Randomized, Parallel-Group Trial to Compare the Efficacy and Safety of Three Doses of Meloxicam (7.5, 15, and 22.5 mg) and Placebo in Patients With Rheumatoid Arthritis
Study Start Date :
Jun 1, 2002
Study Completion Date :
Jul 1, 2003

Outcome Measures

Primary Outcome Measures

  1. Response according to American College of Rheumatology 20% (ACR20) classification [at 12 weeks]

Secondary Outcome Measures

  1. Number of painful or tender joints [up to 12 weeks]

  2. Number of swollen joints [up to 12 weeks]

  3. Patient's global (overall) assessment of disease activity [up to 12 weeks]

  4. Investigator's global (overall) assessment of disease activity [up to 12 weeks]

  5. Patient's assessment of pain [up to 12 weeks]

  6. Patient's assessment of physical function (mHAQ) [up to 12 weeks]

  7. C-Reactive Protein (CRP) [up to 12 weeks]

  8. Withdrawal due to lack of efficacy [up to 12 weeks]

  9. Duration of morning stiffness [up to of 12 weeks]

  10. Patient's final global (overall) assessment of efficacy [at end of 12 weeks]

  11. Investigator's final global (overall) assessment of efficacy [at end of 12 weeks]

  12. Patient status with regard to change in arthritic condition [at end of 12 weeks]

  13. Use of rescue medication [up to 12 weeks]

  14. Incidence and intensity of adverse events [until 4 weeks post treatment]

  15. Patient's final global assessment of tolerability [at end of 12 weeks]

  16. Investigator's final global assessment of tolerability [at end of 12 weeks]

  17. Withdrawals due to adverse events [at end of 12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age greater than or equal to 18 and less than or equal to 80

  • Diagnosis of Rheumatoid Arthritis for at least six weeks

  • Taking an NSAID

  • If female: using adequate contraception

  • Willingness to stop current NSAID until criteria reached to begin study drug

  • Able to provide written informed consent

Exclusion Criteria:
  • Intolerance or hypersensitivity to NSAIDs or ingredients of trial drug

  • Pregnancy, lactating

  • Use of investigational drug within 30 days prior to entering the trial

  • History of peptic ulcer or of gastrointestinal hemorrhage except simple hemorrhoidal bleeding

  • History of cerebrovascular or other bleeding disorder

  • Severe hypertension

  • Other disease that might interfere with safety of the patient or evaluation of trial drug (investigator's opinion)

  • RA of functional class IV

  • Synovectomy in any large joint within the past 6 months prior to entering the trial or planned during trial

  • Concomitant therapy with anticoagulant, therapeutic doses of aspirin, phenothiazines, lithium, chronic GI-medication, analgesic drug (except acetaminophen up to 4 grams/day)

  • DMARDs initiated within past three months or dose changed less than two months before entering the trial

  • Therapy with corticosteroids exceeding 10 mg/day prednisone equivalent or change in dose within 1 month before trial

  • Concomitant therapy with ACTH within past month before entering the trial.

  • History of narcotic or alcohol abuse (past 12 months)

  • Abnormal laboratory values

  • Previous participation in the present trial

Contacts and Locations

Locations

Site City State Country Postal Code
1 Suites 570 (research) & 600 (PI) Huntsville Alabama United States 35801
2 Suite 200 Montgomery Alabama United States 36106
3 Suite 140 Anchorage Alaska United States 99508
4 #106 Glendale Arizona United States 85308
5 Suite 601 Phoenix Arizona United States 85012
6 Suite 201 Phoenix Arizona United States 85015
7 Boehringer Ingelheim Investigational Site Los Angeles California United States 90048
8 Boehringer Ingelheim Investigational Site Pasadena California United States 91105
9 Suite 100 Rancho Cucamonga California United States 91730
10 Boehringer Ingelheim Investigational Site Rancho Mirage California United States 92270-4469
11 Suite 208 San Diego California United States 92108
12 Suite 202 San Diego California United States 92120
13 Suite 301 San Leandro California United States 94578
14 Suite A Santa Maria California United States 93454
15 Westlake Medical Research Westlake Village California United States 91361
16 Suite 200 Colorado Springs Colorado United States 80910
17 Suites 205 & 206 Danbury Connecticut United States 06810
18 Suite 300 Washington District of Columbia United States 20006
19 Boehringer Ingelheim Investigational Site Del Ray Beach Florida United States 33484
20 Boehringer Ingelheim Investigational Site Gainsville Florida United States 32607
21 Boehringer Ingelheim Investigational Site Jacksonville Florida United States 32204
22 Boehringer Ingelheim Investigational Site Largo Florida United States 33773
23 Suite 202 Miami Florida United States 33173
24 Boehringer Ingelheim Investigational Site Ocala Florida United States 03474
25 Renstar Medical Research Ocala Florida United States 34471
26 Boehringer Ingelheim Investigational Site Orlando Florida United States 32804
27 Suite 2 Orlando Florida United States 32806
28 Suite 406 Safety Harbor Florida United States 34695
29 Boehringer Ingelheim Investigational Site Sarasota Florida United States 34239
30 Boehringer Ingelheim Investigational Site South Miami Florida United States 33143
31 Suite 101 St. Petersburg Florida United States 33710
32 Radiant Research Stuart Florida United States 34996
33 Suite 203 Tampa Florida United States 33614
34 Boehringer Ingelheim Investigational Site Zephyrhills Florida United States 33540
35 Boehringer Ingelheim Investigational Site Coeur d'Alene Idaho United States 83814-2644
36 Suite 202 Idaho Falls Idaho United States 83404
37 Boehringer Ingelheim Investigational Site Lake Forest Illinois United States 60045
38 Boehringer Ingelheim Investigational Site Rockford Illinois United States 61103
39 Boehringer Ingelheim Investigational Site Springfield Illinois United States 62704
40 Boehringer Ingelheim Investigational Site Indianapolis Indiana United States 46202
41 Attn: Kathy Stoddard, Director Wichita Kansas United States 67207
42 Suite 306 Wheaton Maryland United States 20902
43 Truesdale Clinic Fall River Massachusetts United States 02720
44 Suite 202 Kalamazoo Michigan United States 49009
45 Suite 101 St. Louis Missouri United States 63128
46 Suite 240 St. Louis Missouri United States 63141
47 Boehringer Ingelheim Investigational Site Lincoln Nebraska United States 68506
48 Boehringer Ingelheim Investigational Site Reno Nevada United States 89502-1196
49 PC, Jackson Commons D-2 Medford New Jersey United States 08055
50 Suite 8 Mercerville New Jersey United States 08619
51 Boehringer Ingelheim Investigational Site New York New York United States 10021
52 Suite 100 Charlotte North Carolina United States 28210
53 Boehringer Ingelheim Investigational Site Columbus Ohio United States 43214
54 Boehringer Ingelheim Investigational Site Tulsa Oklahoma United States 74135
55 Boehringer Ingelheim Investigational Site Camp Hill Pennsylvania United States 17011
56 Altoona Center for Clinical Research Duncansville Pennsylvania United States 16635
57 Boehringer Ingelheim Investigational Site Erie Pennsylvania United States 16508-1256
58 Suite D Mechanicsburg Pennsylvania United States 17055
59 Suite 331-333 Johnston Rhode Island United States 02919
60 Boehringer Ingelheim Investigational Site Columbia South Carolina United States 29204
61 Suite H North Charleston South Carolina United States 29406
62 Boehringer Ingelheim Investigational Site Orangeburg South Carolina United States 29118
63 Boehringer Ingelheim Investigational Site Austin Texas United States 78705
64 Boehringer Ingelheim Investigational Site Dallas Texas United States 75225
65 Radiant Research Dallas Texas United States 75231
66 Suite 200 Dallas Texas United States 75246-1632
67 Suite 500 Lubbock Texas United States 79410
68 Suites 207 San Antonio Texas United States 78217
69 Suite 2A Falls Church Virginia United States 22044
70 Boehringer Ingelheim Investigational Site Everett Washington United States 98201
71 Suite D-3 Seattle Washington United States 98166-2967
72 Boehringer Ingelheim Investigational Site Yakima Washington United States 98902
73 Boehringer Ingelheim Investigational Site Buenos Aires Argentina 1405
74 Boehringer Ingelheim Investigational Site Buenos Aires Argentina 1427
75 Boehringer Ingelheim Investigational Site Buenos Aires Argentina 1428
76 Boehringer Ingelheim Investigational Site Rosario Argentina 2000
77 Boehringer Ingelheim Investigational Site Cotton Tree Queensland Australia 4558
78 Emeritus Research Malvern Victoria Australia 3144
79 Department of Rheumatology Perth Western Australia Australia 6004
80 Clinique du Parc Léopold Bruxelles Belgium 1040
81 Medisch Centrum van Huisartsen Leuven Belgium 3000
82 Av Anhanguera 6479 Goiânia GO Brazil 74043-011
83 Rua Ramiro Barcelos 2350 Porto Alegre RS Brazil 90035-003
84 Boehringer Ingelheim Investigational Site São Paulo - SP Brazil 04040-000
85 Clínica de Doenças Parasitárias e Infecciosas-Hospital Dia São Paulo - SP Brazil 04230-000
86 230-6091 Richmond British Columbia Canada V7C 5L9
87 Boehringer Ingelheim Investigational Site Victoria British Columbia Canada V8P 5P6
88 Boehringer Ingelheim Investigational Site Corunna Ontario Canada N0N 1G0
89 Boehringer Ingelheim Investigational Site Fort Erie Ontario Canada L2A 1Z3
90 Boehringer Ingelheim Investigational Site Hamilton Ontario Canada L8N 1Y2
91 Dr. Denis O'Donnell Kingston Ontario Canada K7L 2V6
92 Trillium Health Centre Mississauga Ontario Canada L5B 4A2
93 Boehringer Ingelheim Investigational Site Ottawa Ontario Canada K2P 1V3
94 Boehringer Ingelheim Investigational Site Peterborough Ontario Canada K9J 7H8
95 Boehringer Ingelheim Investigational Site Sarnia Ontario Canada N7T 4X3
96 Boehringer Ingelheim Investigational Site Scarborough Ontario Canada M1B 4Y9
97 104-532 St. Catharines Ontario Canada L2N 4H4
98 Boehringer Ingelheim Investigational Site Toronto Ontario Canada M3B 2H9
99 Boehringer Ingelheim Investigational Site Windsor Ontario Canada N8W 5L7
100 Boehringer Ingelheim Investigational Site Montreal Quebec Canada H3G 1A4
101 Boehringer Ingelheim Investigational Site Montreal Quebec Canada H3Z, 2Z3
102 Boehringer Ingelheim Investigational Site Pointe-Claire Quebec Canada H9R 3J1
103 Boehringer Ingelheim Investigational Site Marseille France 13008
104 Boehringer Ingelheim Investigational Site Nice France 06000
105 Boehringer Ingelheim Investigational Site Tours cedex 9 France 37044
106 Boehringer Ingelheim Investigational Site Tours France 37000
107 Boehringer Ingelheim Investigational Site Aachen Germany 52064
108 Augusta-Klinik Bad Kreuznach Germany 55543
109 Boehringer Ingelheim Investigational Site Bad Segeberg Germany 23795
110 Rheumatologie und Physikalische Therapie Berlin Germany 14059
111 Boehringer Ingelheim Investigational Site Ellefeld Germany 08236
112 Elisabeth-Krankenhaus Essen Germany 45356
113 Boehringer Ingelheim Investigational Site Klotten Germany 56818
114 ClinPharm International GmbH & Co. KG Leipzig Germany 04229
115 Boehringer Ingelheim Investigational Site München Germany 81541
116 Boehringer Ingelheim Investigational Site Nürnberg Germany 90402
117 Boehringer Ingelheim Investigational Site Nürnberg Germany 90461
118 Boehringer Ingelheim Investigational Site Steinhöring Germany 85643
119 Boehringer Ingelheim Investigational Site Tübingen Germany 72070
120 Klinik für Rheumatologie, Wiesbaden Germany 65191
121 National Institute for Rheumatology and Physiotherapy Budapest Hungary 1027
122 DOTE Debrecen Hungary 4031
123 Aladár Petz County Hospital Györ Hungary 9024
124 St. Andrew State Hospital Hévíz Hungary 8380
125 St. Ferenc Hospital Miskolc Hungary 3501
126 Hungarian Brothers of St. John of Good Pecs Hungary 7621
127 Szegedi University Szeged Hungary 6720
128 Ferenc Csolnoky County Hospital Veszprem Hungary 8201
129 Pál Almási Balogh Hospital Ózd Hungary 3601
130 Università degli Studi Genova Italy
131 Ospedale Augusto Murri Jesi Italy 60035
132 Università degli Studi di Napoli "Federico II" Napoli Italy 80131
133 Ospedale A. Galateo SAN CESARIO (Lecce) Italy 73016
134 896 Pyung Chon-Dong, Dongan-Gu Gyeonggi-Do Korea, Republic of 431-070
135 San-5, Woncheon-Dong, Paldal-Gu Gyeonggi-Do Korea, Republic of 442-721
136 85 Jeo-Dong 2Ga Seoul Korea, Republic of 100-032
137 Seoul National University Hospital Seoul Korea, Republic of 110-744
138 Boehringer Ingelheim Investigational Site Seoul Korea, Republic of 120-752
139 Institute of Rheumatology of RAMN Moscow Russian Federation 115522
140 City Clinical Hospital No. 1 Moscow Russian Federation 117049
141 Kaohsiung Medical University Chung-Ho Memorial Hospital Kaohsiung Taiwan
142 Rheumatology-Allergy-Immunology Kaohsiung Taiwan
143 Chang Gung Memorial Hospital Taipei Taiwan 105
144 Taipei Veterans General Hospital Taipei Taiwan
145 Dnyepropyetrovsk Medical Academy Dnyepropetrovsk Ukraine 49044
146 Central City Hospital Donetsk Ukraine 83098
147 State Medical University Donetsk Ukraine 83114
148 Municipal Institute of Health Care Kharkov Ukraine 61091
149 City Multitype Clinical Hospital No. 25 Kharkov Ukraine 61115
150 Central Clinical Hospital Kiev Ukraine 01023
151 Institute of Cardiology Kiev Ukraine 03151
152 Regional Hospital No. 1 Kiev Ukraine 04107
153 Institute of Gerontology Kyiv Ukraine 04114

Sponsors and Collaborators

  • Boehringer Ingelheim

Investigators

  • Study Chair: Boehringer Ingelheim Study Coordinator, Boehringer Ingelheim Ltd./Bracknell

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00042068
Other Study ID Numbers:
  • 107.258
First Posted:
Jul 24, 2002
Last Update Posted:
Nov 1, 2013
Last Verified:
Oct 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 1, 2013