Trial Details
AuthorisedBasic Information
| Clinical ID | c2586 |
|---|---|
| Identifier | EUCTR2018-002982-20-GB |
| Trial Title | A Pilot Study to assess the efficacy and safety of reduced dose oral iron in the treatment of iron deficiency anaemia in inflammatory bowel disease patients - Efficacy and safety of low dose oral iron for anaemia in IBD (CAESAR) |
| Trial URL | Visit Original Page |
Study Information
| Study Results | No results available |
|---|---|
| Conditions | Iron deficiency anaemia in inflammatory bowel disease MedDRA version: 20.0_Level: LLT_Classification code 10002062_Term: Anaemia iron deficiency_System Organ Class: 100000004851_ MedDRA version: 20.1_Level: PT_Classification code 10021972_Term: Inflammatory bowel disease_System Organ Class: 10017947 - Gastrointestinal disorders_;Therapeutic area: Diseases [C] - Digestive System Diseases [C06] |
| Interventions | Trade Name: Ferrous Fumarate Syrup Product Name: Ferrous Fumarate Syrup Product Code: Ferrous fumarate syrup Pharmaceutical Form: Syrup INN or Proposed INN: Ferrous fumarate CAS Number: 141-01-5 Current Sponsor code: NA Other descriptive name: NA Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration number: 140mg-5ml |
Participant Information
| Sponsor | Royal Liverpool University Hospital |
|---|---|
| City | - |
| Country/Region | United Kingdom |
Enrollment Criteria
| Sex Requirement | NOT SPECIFIED |
|---|---|
| Age Requirement | - |
Study Design
| Study Type | Interventional clinical trial of medicinal product |
|---|---|
| Phase | PHASE4 |
Time Information
| Start Date | 2025-04-24 |
|---|---|
| Primary Completion Date | - |
| Completion Date | - |