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A clinical trial to study the effect of two different routes (nasal and parenteral) of administration of a drugs, vitamin B12, in patients with macrocytic anemia

Phase 3
Conditions
Health Condition 1: D519- Vitamin B12 deficiency anemia, unspecified
Registration Number
CTRI/2023/09/058162
Lead Sponsor
Command Hospital Central Command
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Hemoglobin < 13g/dL male, <12g/dL female.

2.Mean corpuscular volume >100 fL.

3.Normal Transferrin saturation.

4.Should not have any comorbidities causing anemia.

Exclusion Criteria

Patients with macrocytic anemia having any of the following characteristics will be excluded

1.Patients receiving other modalities of treatment and/or alternative medicine.

2.Patients who did not consent for the study.

3.Rhinitis.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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