Skip to content

Preoperative Vitamin B12 and Folic Acid on POCD in Elderly Non-cardiac Surgical Patients

Effect of Preoperative Vitamin B12 on Post Operative Cognitive Dysfunction in Elderly Patients Undergoing Non-cardiac Surgery: A Multi-Center, Prospective, Randomized, Double-blinded, Controlled Clinical Trial

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03485404
Acronym
B12-POCD
Enrollment
40
Registered
2018-04-02
Start date
2019-01-10
Completion date
2021-07-29
Last updated
2021-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Cognitive Dysfunction

Keywords

POCD, vitamin B12, folic acid

Brief summary

This study will recruit patients more than 65 years old eligible for non-cardiac surgery. Patients who participate will take either vitamin B12 and folic acid supplementation or placebo for 7 days before surgery. Neuropsychological test battery (NPB) will be tested before intervention and at discharge for determination of Post operative cognitive dysfunction (POCD). Another group of non-surgical elderly participants will also be tested for NPB to account for learning effect in POCD diagnosis. The hypothesis is that preoperative vitamin B12 supplementation will reduce the incidence of POCD in elderly patients undergoing non-cardiac surgery.

Detailed description

Vitamin B12 has long been suggested to have neural nutrient effect and widely used in clinical settings for patients with peripheral nerve injury as well as complementary medicine for patients with CNS disorders, including cognitive dysfunction. Evidences showed that, although no significant improvement in cognitive function was observed in healthy elderly after vitamin B12 supplementation, some studies suggested that patients with pre-existing CNS disorder may benefit from Vitamin B12. Post operational cognitive dysfunction (POCD) is severe, and long-lasting complication that affects as high as 53% of patients in high risk surgeries. Age is an independent risk factor for POCD. Researches have shown that serum vitamin B12 level decrease with age, and methylcobalamin (active form of Vitamin B12) content in the frontal cortex of aged patients are lower than that of younger patients. However, there are no report on effect of preemptive supplementation of vitamin B12 on POCD incidence. Therefore, the current research is aimed to explore the preoperative methylcobalamin supplementation (500 mg, 3/day for 7 days before surgery) on incidence of POCD. Folic acid supplementation is a common companion for vitamin B12 treatment in clinical settings because they are in the same methionine cycle, increase of one may result in deficiency of another. So we added 5 mg, 1/day of folic acid with methylcobalamin in the treatment group. This study will recruit patients more than 65 years old eligible for non-cardiac surgery. Patients who participate will take either vitamin B12 and folic acid supplementation or placebo for 7 days before surgery. Neuropsychological test battery (NPB) will be tested before intervention and at discharge for determination of Post operative cognitive dysfunction (POCD). Another group of non-surgical elderly participants will also be tested for NPB to account for learning effect in POCD diagnosis. The hypothesis is that preoperative vitamin B12 supplementation will reduce the incidence of POCD in elderly patients undergoing non-cardiac surgery.

Interventions

methylcobalamin tablets, 0.5mg/tablet, 3 tablets/day.

DRUGFolic Acid

folic acid tablets, 5mg/tablet, 1 tablet/day

OTHERPlacebo for methylcobalamin

orange tablets that looks exactly like methylcobalamin

OTHERPlacebo for folic acid

yellow tablets that looks exactly like folic acid

PROCEDUREnon-cardiac surgery

patients elective for non-cardiac surgery will undergo scheduled surgery after 7 days of intervention

BEHAVIORALNPB test

participants will accept Mini-Mental State Examination (MMSE), Patient Health Questionnaire (PHQ-9), ADL, and NPB test before intervention, and NPB by discharge or similar time intermittent after the first assessment for non-surgical controls. Also ADL will be tested again through telephone interview at 3 months after discharge.

Sponsors

First Affiliated Hospital Xi'an Jiaotong University
CollaboratorOTHER
Tang-Du Hospital
CollaboratorOTHER
Shaanxi Provincial People's Hospital
CollaboratorOTHER
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
CollaboratorOTHER
Anhui Provincial Hospital
CollaboratorOTHER_GOV
Shanghai 10th People's Hospital
CollaboratorOTHER
Xijing Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Masking description

Central randomization. Groups are marked as A and B with no participants, care provider, investigator and outcome assessors know which group is the drug and which is the placebo. Placebo are made as tablets that mimics the color, shape and size of the drugs.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 1\. Age equals or over 65 * 2\. Scheduled for spinal or joint replacement surgery under general anesthesia,estimated surgery time over 2h. * 3\. Signed written informed consent obtained * 4\. Non-surgical Controls are age and sex - matched community elderly residents.

Exclusion criteria

* 1\. Disease of the central nervous system that impairs cognitive function, including all kinds of dementia, and depression * 2\. MMSE score \< 24 * 3\. Received education for less than 5 years * 4\. Currently taking sedative or antidepressant drugs * 5\. Has taken vitamin B12, folic acid or their derivatives (methycobalamin, cobalamin, tetrahydrofolic acid, etc.) within 6 months. * 6\. Has accepted cardiac or neurological surgery within one year. * 7\. Was admitted for other clinical trials within 3 month * 8\. Patients that regularly taking drugs that affect vitamin B absorption, including colchicine, neomycin, salicylate. * 9\. Has severe visual or auditory problems * 10\. Alcohol or drug dependent (alcohol dependent: drank more than 100 mL of Chinese liqueur with alcohol concentration over 40% everyday for the past 3 months). * 11\. Patients that are already admitted for this study can not be admitted the second time, no matter the cause of surgery

Design outcomes

Primary

MeasureTime frameDescription
Incidence of POCD at discharge or 7 days after operationat discharge or at 7 days after operation if the patient is not discharged by thenPOCD incidence is defined as two or more test of the neuropsychological battery declined as compared to preoperative baseline.

Secondary

MeasureTime frameDescription
Activity daily living score3 months after operationTelephone interview of activity daily living score (14 items, 1-4 points per item, ranging 14-56 points with 56 being the worst-unable to complete any task of everyday living.)
Serum level of vitamin B12, folic acid and homocysteineImmediately before anesthesia, immediately after surgery and on the morning of postoperative day 1Ten ml of venous blood will be collected from patients to test the differences of serum levels of vitamin B12, folic acid and homocysteine to show the effect of preoperative supplementation and surgery stimulation on these parameters.
Serum level of cystatin C and myeloid differentiation protein 2Immediately before anesthesia, immediately after surgery and on the morning of postoperative day 1Ten ml of venous blood will be collected from patients to test the differences of serum levels of cystatin C and myeloid differentiation protein 2.
Length of hospital stayDate from hospital admission to hospital discharge. This length is usually around 7-14 days. It may be longer if the patient have one or more complications. The length will be documented at patient discharge, up to 100 weeks.to see if our intervention could reduce the total days of patient spent in hospital,
Incidence of in hospital complicationsFrom date of hospital admission to date of hospital discharge after surgery. Usually 7-14 days, assessed up to 100 weeks.Overall rate of perioperative major complications including hemorrhage, deep vein thrombosis, cardiovascular complications, respiratory complications, acute kidney injury, infection or second operative needed, during patient's hospital stay.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026