General information Section to complete general information about the trial: scientific and public title, protocol identifiers, sponsors and Source(s) of Monetary or Material Support.
Scientific title:
Evaluation of the efficacy and safety of Combifer T compared to Trofin and Ferrous fumarate in the treatment of iron deficiency anemia in pregnant women.
Secondary indentifying numbers:
Issuing authority of the secondary identifying numbers:
National Center of Bioproducts (BioCen)
Source(s) of monetary or material support:
National Center of Bioproducts (BioCen)Ministry of Public Health (MINSAP)
Authorization for beginning Section to complete information about the regulatory approval of clinical trial: regulatory agency name, approval date and reference number in the agency.
Regulatory instance to authorize the initiation of the study:
Center for State Control of Drugs, Medical Devices and Equipment (CECMED)
Principal investigator Section to complete information about Email address, telephone number and postal address of the Principal Investigator.
Medical Specialty :
Specialist of second degree in Gynecology and Obstetrics, Consultant Professor. MsC Integral Care for Women
Affiliation:
Docent Gyneco-Obstetric Hospital 10 de Octubre, Daughters of Galicia.
Postal address:
Our Lady of Rule No. 52 between Remedios and Quiroga, Luyano. October 10th.
Clinical sites to participate Section to complete the data related to the clinical sites involved in the trial: site and responsible investigator for every site.
Countries of recruitment:
Clinical sites:
Havana, Mother House "Leonor Perez Cabrera", Yeilin Pereira Minnoz, MD , Specialist of first Degree in Gynecology and Obstetric.
Havana, Docent Gyneco-Obstetric Hospital America Arias Yuribet Borges Moreno, MD, Specialist of first Degree in Hematology.
Research ethics committees:
Docent Gyneco-Obstetric Hospital 10 de Octubre, Daughters of Galicia, in review.
Mother House “Leonor Perez Cabrera” , in review.
Docent Gyneco-Obstetric Hospital America Arias , in review.
Recruitment status Section to complete information about the recruitment status and the date of first enrolment subject
Date of first enrollment:
Health condition and Intervention Section to complete information about the primary medical condition(s) or problem(s) studied and, a characteristics of the intervention(s).
Health condition(s) or Problem(s) studied:
Health condition(s) code:
Hematinics
Anemia
Hematologic Diseases
Hemic and Lymphatic Diseases
Iron Deficiency
Intervention(s):
Group I - Combifer (Experimental): a tablet of Combifer (500mg) by oral route 3 times a day, 30 minutes before breakfast, lunch and dinner. The tablets will be administered from enrollment in the study until the end of pregnancy.
Group II - Trofin (Control): A tablespoon of Trofin (15mL) by oral route 3 times a day, 30 minutes before breakfast, lunch and dinner. The medication will be administered from enrollment in the study until the end of pregnancy.
Group III - Ferrous Fumarate (Control): A tablet of Ferrous Fumarate (200mg) by oral route 2 times a day, 30 minutes after breakfast and lunch. The tablets will be administered from enrollment in the study until the end of pregnancy.
Intervention code:
Iron, Dietary
Biological Products
Dietary Supplements
Tablets
Administration, Oral
Intervention keyword:
Ferrous fumarate,
Combifer,
Trofin
Outcomes and Timepoint Section to complete information about primary and secondary outcomes including. It includes the metric or method of measurement used and, the time point for every outcome.
Primary outcome(s):
Hemoglobin (g/L). Measurement time: At baseline and, every 4 weeks until the end of pregnancy.
Key secondary outcomes:
1. Hematocrit (%). Measurement time: At baseline and, every 4 weeks until the end of pregnancy.
2. Serum iron (μg / dL). Measurement time: At baseline and, every 4 weeks until the end of pregnancy.
3. Reticulocytes (x 10-3). Measurement time: At baseline and, every 4 weeks until the end of pregnancy.
4. Ferritin (ng/mL). At baseline and, every 4 weeks until the end of pregnancy.
5. Peripheral lamina (size, shape and color of red blood cells). Measurement time At baseline and, every 4 weeks until the end of pregnancy.
6. Average Corpuscular Volume (fL). Measurement time: At baseline and, every 4 weeks until the end of pregnancy.
7. Corpuscular Media Hemoglobin (pq). Measurement time: At baseline and, every 4 weeks until the end of pregnancy.
8. Concentration of Corpuscular Hemoglobin Medium (g/L). At baseline and, every 4 weeks until the end of pregnancy.
9. Adverse Events-AE (Occurrence of some AE in the subject (Yes, No); Type of AE (Name of the adverse event); Time of appearance (Immediate, Mediate, Delayed); Duration of the AE (hours and minutes, days); Prior knowledge (Expected, Unexpected); Intensity of the AE (Mild, Moderate, Severe); Consequence of the AE (Serious, Not serious); Causality Relationship (1. Very likely, 2. Probable, 3. Possible, 4. Not likely, 5. Not related, 6. Not evaluable); Result of the AE (Recovered, Not Recovered, Recovered with squeals, Death, Unknown); Attitude regarding the treatment under study (Continuation, Definitive interruption)). Measurement time: each administration of the product and during the entire duration of the test.
Selection criterias Section to complete information about the inclusion and exclusion criteria for participant selection, including age and gender.
Inclusion criteria:
1. Patients who have given their informed consent to participate in the trial.
2. Patients with pregnancy between 15 and up to 24 weeks of gestation.
3. Patients with hemoglobin levels between 75 and 109 g/L.
Exclusion criteria:
1. Patients with acute gastrointestinal disorders (vomiting, diarrhea).
2. Patients who received transfusions during pregnancy.
3. Pregnant women with hypertension who have indicated Methyldopa since Ferrous Fumarate reduces the hypotensive effect of Methyldopa.
4. Patients under treatment with iron dextran or who received treatment one month before the start of the study.
Study design Section to complete information about the characteristics of the study design.
Allocation:
Randomized controlled trial
Contact for public queries Section to complete information about Email address, telephone number and postal address of the contact who will respond to general queries, including information about current recruitment status
Specialty:
Specialist of second Degree in Gynecology and Obstetrics, Consultant Professor. MsC Integral Care for Women
Affiliation:
Teaching Gyneco-Obstetric Hospital 10 de Octubre, Daughters of Galicia.
Postal Address:
52 Our Lady of Rule between Remedios and Quiroga, Luyano. October 10th.
Contact for scientific queries Section to complete information about Email address, telephone number and postal address of the contact who will respond to scientific queries.
Specialty:
BSc. Pharmaceutic Science
Affiliation:
National Center of Bioproducts, BioCen
Postal Address:
Road to Beltran Km 1 ½, Bejucal
Telephone:
+53-47682201-07 ext 1145 and 1147
Data Sharing Section to complete the data related to the data sharing plan.
Registration and Update Section to complete information about the name of Primary Registry, date of registration and the unique ID number assigned by the registry (RPCEC).
Date of Registration in Primary Registry:
Record Verification Date:
Link to the spanish version:
