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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  
Name  Address 
NIL  NIL 
 
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  
Status 
Not Applicable 
 
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.

 
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