| CTRI Number |
CTRI/2024/09/073346 [Registered on: 04/09/2024] Trial Registered Prospectively |
| Last Modified On: |
02/09/2024 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Surgical/Anesthesia |
| Study Design |
Randomized, Parallel Group, Active Controlled Trial |
|
Public Title of Study
|
Comparing the benefits of treatment with iron tablet vs iron injections in reducing need for blood during operations of food pipe cancers in patients with anemia due to the lack of iron in the body |
|
Scientific Title of Study
|
Evaluating the relative efficacy of preoperative intravenous vs oral iron supplementation in reducing perioperative allogenic blood transfusions in patients of gastrointestinal malignancies with iron deficiency anemia: a randomised controlled trial |
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Manyata Nema |
| Designation |
Senior Resident |
| Affiliation |
Dr. BRAIRCH, AIIMS, New Delhi |
| Address |
Department of Onco-Anaesthesia and Palliative Medicine,
Dr. BRA IRCH, AIIMS, New Delhi
Ansari Nagar
New Delhi DELHI 110029 India |
| Phone |
7619488327 |
| Fax |
|
| Email |
manyatanema16896@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Prof. Sachidanand Jee Bharati |
| Designation |
Professor |
| Affiliation |
Department of Onco-Anaesthesia and Palliative Medicine, Dr. BRAIRCH, AIIMS, New Delhi |
| Address |
Department of Onco-Anaesthesia and Palliative Medicine, Dr. BRAIRCH, AIIMS, New Delhi
Ansari Nagar
New Delhi DELHI 110029 India |
| Phone |
9968436042 |
| Fax |
|
| Email |
sachidadr@yahoo.co.in |
|
Details of Contact Person Public Query
|
| Name |
Dr Manyata Nema |
| Designation |
Senior Resident |
| Affiliation |
Dr. BRAIRCH, AIIMS, New Delhi |
| Address |
Department of Onco-Anaesthesia and Palliative Medicine,
Dr. BRA IRCH, AIIMS, New Delhi
Ansari Nagar
New Delhi DELHI 110029 India |
| Phone |
7619488327 |
| Fax |
|
| Email |
manyatanema16896@gmail.com |
|
|
Source of Monetary or Material Support
|
| AIIMS New Delhi
Ansari Nagar, New Delhi, India -110029 |
|
|
Primary Sponsor
|
| Name |
AIIMS New Delhi |
| Address |
Sri Aurobindo Marg,
Ansari Nagar East,
New Delhi 110049 |
| Type of Sponsor |
Government medical college |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Manyata Nema |
AIIMS New Delhi |
Department of Onco-Anaesthesia and Palliative Medicine, Dr BRAIRCH, AIIMS New Delhi New Delhi DELHI |
7619488327
manyatanema16896@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| INSTITUTE ETHICS COMMITTEE FOR POST GRADUATE RESEARCH, ALL INDIA INSTITUTE OF MEDICAL SCIENCES, ANSARI NAGAR, NEW DELHI |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: O||Medical and Surgical, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
IV IRON |
These patients will receive the calculated dose of iron (as per the deficit calculation done using the Ganzoni formula) using intravenous injection Ferric carboxymaltose solution in 1-2 divided dosages over 2 weeks, with the 1st dose being administered at least 4 weeks prior to the scheduled date of surgery.
Total Duration of the treatment is 1-2 days, depending on the dose required for a particular patient |
| Comparator Agent |
Oral Iron |
These patients will receive oral iron preparation in the form of Ferrous Sulfate tablets 200 mg twice daily for the entire pre-operative period, starting from the day of enrolment (at least 4 weeks prior to the scheduled date of surgery).
The duration of the treatment will be at 4 weeks. |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
99.00 Year(s) |
| Gender |
Both |
| Details |
ASA class I-III, scheduled to undergo elective surgeries for gastro-intestinal malignancies at least 4 weeks after presenting to the OPD with iron deficiency anemia
|
|
| ExclusionCriteria |
| Details |
Patients who are on oral iron therapy at the time of recruitment or erythropoietin within 12 weeks before recruitment
Patients with symptomatic anemia requiring blood transfusions
Anemia due to vitamin B12 or folate deficiency, hemolytic diseases, hemoglobinopathies or thalassemia
Patients who have known allergy/ hypersensitivity to any of the study drugs
Patients who are unable to take orally
Unoptimized reactive airway diseases, not on inhaled corticosteroids
Patients with chronic renal failure
Patients with untreated hypophosphatemia, vitamin D deficiency and hyperparathyroidism (in view of anticipated fractures)
Pregnant patients
|
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Sequentially numbered, sealed, opaque envelopes |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
| The incidence of allogenic blood transfusions required in the perioperative period |
from enrolment till post-operative day 1 |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| The total number of units of packed red blood cell transfusions required in the perioperative period |
from enrolment till post-operative day 1 |
| The changes in hemoglobin concentration from the baseline (at enrolment) between the two groups at two different time points |
on the day before surgery and on post-operative day 1 |
| The serum ferritin levels and the percentage transferrin saturation between the two groups at two different time points [as compared to baseline] |
day before surgery and on post-operative day 1 |
| Adverse reactions |
During Intravenous Iron administration and during surgery |
|
|
Target Sample Size
|
Total Sample Size="114" Sample Size from India="114"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
Phase 3/ Phase 4 |
|
Date of First Enrollment (India)
|
16/09/2024 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="1" Months="6" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Gastrointestinal malignancies (including cancers of the esophagus, stomach, small intestine, colon, rectum and anal canal) account for a significant proportion of the total cancer burden in India (about 11 – 12 % in either sexes). Patients with gastrointestinal malignancies posted for definitive surgeries often present with anemia- mostly absolute and/or functional iron deficiency anemia – with a reported incidence of around 40% . The causes of anemia in this population are usually multi-factorial – either primarily due to the cancer (40% of the total) or, secondary to the chemotherapeutic agents used for treating the cancer (60%). Irrespective of the etiology, cancer related anemia decreases the patient’s quality of life, decreases the efficacy and tolerance to the anti-cancer therapies and often causes delay in definitive surgeries. Treatment options for pre-operative iron deficiency anemia is usually guided by the severity and the available time for optimization – and includes, oral and IV iron supplementation, erythropoietic agents and blood transfusions. Given the time-sensitive nature of onco-surgeries, often peri-operative blood transfusions are done to optimize the hemoglobin concentrations within a short period of time. However, concerns regarding transfusion-related immuno-modulation (TRIM), and circulatory overload often pose a clinical dilemma regarding the appropriateness of allogenic blood transfusions in cancer patients. Erythropoietic agents are usually contraindicated due to risks of thromboembolic events and myelodysplastic syndromes . Studies have shown a slower than desired hemoglobin buildup with oral iron supplementation along with poor tolerability. On the other hand, intravenous iron supplementation carries an inherent risk of allergic reactions ranging from urticaria to anaphylactic shock as well as iron overload due to presence of functional iron deficiency (low circulating iron levels despite adequate stores) in malignancies. The current evidence on the comparative efficacy of intravenous vs oral iron supplementation in reducing peri-operative blood transfusions is conflicting. While, most studies show a significant improvement in hemoglobin concentrations at least 4 weeks after intravenous iron administration, the evidence regarding its efficacy in reducing perioperative blood transfusion is conflicting. Some studies report a reduction is the need for allogenic blood transfusions, while others did not report any significant difference in transfusion requirements. This contradictory data could be partly explained by the fact that different studies included variety of patient populations – both malignant and non-malignant, and some did not even ensure that the anemia is actually due to iron deficiency. Also, the time to assess the outcome measures varied from 2-4 weeks from the point of intravenous iron administration, while it is almost evident that the response to intravenous iron starts manifesting from 4 weeks onwards. Hence, we designed this RCT to evaluate the efficacy of intravenous iron (when administered at least 4 weeks prior to elective surgeries for gastrointestinal malignancies) in patients with iron deficiency anemia in reducing the need for allogenic blood transfusion peri-operatively, as compared to our current institutional practice of administering oral iron preparations. |