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Vitamin B 12 Deficiency clinical trials

View clinical trials related to Vitamin B 12 Deficiency.

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NCT ID: NCT06441721 Not yet recruiting - Clinical trials for End Stage Renal Disease on Dialysis

Vitamin B12 Status and Its Impact on Chronic Haemodialysis Patient

Haemodialysis
Start date: July 5, 2024
Phase:
Study type: Observational

To evaluate vitamin B12 level in haemodialysis patients and its impact on hematological and neurological manifestations

NCT ID: NCT06376591 Not yet recruiting - Clinical trials for Vitamin B 12 Deficiency

Assessing the Efficacy of Different Carrier Systems in Oral Vitamin B12 Supplementation in Healthy Adults With B12 Deficiency

Start date: April 22, 2024
Phase: N/A
Study type: Interventional

Vitamin B12, a vital nutrient, plays a crucial role in red blood cell formation, neurological function, and DNA synthesis. Deficiency in B12 can lead to anemia, neurological symptoms such as tingling or numbness, and cognitive impairment. Oral B12 supplementation serves as an effective strategy to address B12 deficiency, especially for individuals with limited dietary intake or absorption issues. Regular B12 supplementation can help restore body B12 levels, alleviate deficiency-related symptoms, and support overall health and well-being.

NCT ID: NCT06046703 Not yet recruiting - Pregnancy Clinical Trials

Diet Quality of Pregnant Women With a Strict Plant-based Diet Versus an Omnivorous Diet

Start date: January 1, 2025
Phase:
Study type: Observational

The goal of this observational study is to compare the nutritional intake among pregnant women with a strict plant-based diet versus an omnivorous diet. The main aim is to compare vitamin B12 intake. Participants will be asked to: - fill out a health questionnaire - fill out a three-day food diary - undergo blood sampling Researchers will compare pregnant women with a strict plant-based diet and pregnant women with an omnivorous diet to see if their nutritional intake is comparable.

NCT ID: NCT05714917 Not yet recruiting - Paresthesia Clinical Trials

Neurological Recovery Following NOS-SACD

Start date: April 1, 2023
Phase:
Study type: Observational

Nitrous oxide has become an increasingly popular recreational drug amongst young people, particularly at festivals, nightclubs and parties. Considering the drug is not illegal to possess, has low cost in the form of 'whippets' and can be easily purchased online, it has become the second most commonly used recreational drug amongst people aged 16-24 in the UK. However, nitrous oxide is known to irreversibly inactivate the functioning of vitamin B12, a vitamin required for the maintenance and proper functioning of nerves in the spinal cord. Neurological symptoms in this population have been reported in around 3.4% of nitrous oxide users, although the true incidence is expected to be higher as the cases being reported by UK hospitals continues to rise. Patients may present with adverse neurological symptoms like tingling, weakness, coordination and mobility problems. Currently, studies reviewing the functional recovery of these patients have been limited by a retrospective study design, short follow up duration and being limited to small cohort sizes. This is in part linked to patient non-compliance and non-attendance at follow-up appointments. The investigators will therefore prospectively recruit all patients presenting with these symptoms and continue to collect data relating to their neurological recovery for 12 months. Data collection will be remote to ensure it is of low burden to the participants. This will allow the investigating team and others to fully appraise the severity of these toxic neuropathies and understand how best to manage their follow up.