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CompletedNCT04554082Updated Sep 18, 2020

Evaluation of Micronutrients in Obese Patients

An observational study in Nutritional Disorder, sponsored by Alexandria University. Completed. Open to participants aged 20 Years to 55 Years. Per ClinicalTrials.gov, last updated 2020-09-18.

Sponsored by Alexandria University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
107
Ages
20 Years to 55 Years
Sex
All
01

Study summary

The aim of the study primarily was to investigate the value of zinc to copper ratio as possible biomarker of trace elements imbalance in morbidly obese subjects undergoing LSG.

Secondly to correlate zinc to copper ratio with lipocalin 2 (Lcn2) with respect to Anthropometric measurements and other metabolic biomarkers.

Prospective study will be carried out on 120 morbidly obese adult subjects with a body mass index (BMI) score above 40 along with presence of obesity-related comorbidity. Investigations will be measured preoperative and 9 months postoperative after performing Laparoscopic sleeve gastrectomy; for Body mass index (BMI) and waist circumference. As well as for complete blood count and biochemical biomarkers as fasting blood glucose, lipid profile, serum iron and ferritin. Serum Ceruloplasmin, Zn and Cu levels, followed by calculation of zinc to copper ratio. CRP, serum insulin, serum leptin and lipocalin-2 (Lcn2) will be determined.

Read the detailed description

CONSORT 2010 Flow Diagram

Materials and methods:

Recruitment Morbidly obese subjects attending clinic at Surgery department for laparoscopic sleeve gastrectomy Alexandria University Hospitals.

Pre-assignment Details adult morbidly obese subjects were included age above 20 years, BMI above 40 Suffering from comorbidities as hypertension, DM, dyslipidemia. Assigned participants were clinically evaluated for comorbidities as hypertension, DM, dyslipidemia.

As well as signs of nutritional deficiency as anemia, brittle nails.

Group Information one group of participants eligible for laparoscopic sleeve gastrectomy were assigned according to their will to participate in study.

Period of evaluation:

First visit: preoperative for clinical assessment of participants, determine BMI and waist circumference and withdrawal of serum blood sample Second visit: within one month after surgery to make sure that no complication occurred after surgery.

Third visit: nine months postoperative for revaluation of participants, determine BMI and waist circumference, and withdrawal of a serum blood sample

Number of participants at initiating the period of study. They were 120 morbidly obese subjects. Number of participants at the end of the period of study. They were 107 subjects, 13 obese subject withdraw from study as they didn't come during follow up period after 9 months.

Participants according Sex (69 females, and 38 male), with the mean age of 41.6±8.9 years. The mean preoperative BMI was 47.43±5.4 kg/m2. Then, they were evaluated 9 months after LSG.

Preoperative and Postoperative Clinical characteristics and metabolic variables in studied subjects.

Preoperative 9 months postoperative P Body weight (Kg) 129.7 ± 12.1 93.4 ±13.6 0.0013* BMI (kg/m2) 47.43±5.4 35.7±3.8 0.0052* Waist circumference (cm) 130.00 ± 4.68 91.82 ± 3.73 0.001* Systolic BP (mmHg) 146.0±17.0 132.0±11.0 0.001* Total cholesterol (mmol/L) 5.85 ± 0.41 4.64 ± 0.31 0.035* Triglycerides (mmol/L) 2.20 ± 0.23 1.92 ± 0.24 0.106 HDL cholesterol (mmol/L) 1.23 ± 0.19 1.39 ± 0.2 0.041* LDL cholesterol (mmol/L) 3.37 ± 0.23 2.97 ± 0.21 0.022* HOMA-IR 2.64 ± 1.3 1.44 ± 0.81 0.013* S. Leptin (ng/ml) 102.87 ± 49.16 33.47 ±12.76 0.0001* CRP (mg/L) 8.4±5.91 3.2±2.98 0.001* Lipocalin 2 (µg/L) 107.24±36.8 51.6±12.73 0.001* Albumin (g/dl) 4.05±0.21 3.91±0.29 0.113

*Statistically significant at (p≤0.05).

Outcome measures:

primarily was to investigate the value of zinc to copper ratio as possible biomarker of TE imbalance in morbidly obese subjects undergoing LSG.

For detection of presence of micronutrient deficiency in morbid obesity in form of zinc to copper ratio and re-evaluate it after loss of weight

Secondly to correlate it with lipocalin 2 (Lcn2) with respect to Anthropometric measurements and other metabolic markers prospectively.

As zinc to copper ratio is considered as biomarker of micronutrient status; therefore, correlate it with other biomarkers of inflammation (lipocalin 2) and other parameters as BMI, FBG to determine if micronutrient status improve after weight loss or not Time frame: 9 months.

Follow-up and outcome parameters:

All studied subjects will be followed up for early postoperative complications (within the first month) as Bleeding or Leak. Then they will be reviewed after 9 months postoperatively for assessment of anthropometric measurements, control of preoperative comorbidities, and manifestations of TE deficiencies (anemia, hair loss, teeth problems, edema. etc.).

Anthropometric parameters

Body mass index (BMI) and waist circumference will be measured preoperative and 9 months postoperative.

Biochemical parameters

Fasting blood samples will be collected from participants prior to surgery and nine months postoperative, after overnight fast and divided into two tubes; EDTA for complete blood count, the rest into plastic tubes and serum sample.

Serum glucose and Total cholesterol, HDL- cholesterol, LDL- cholesterol, and triglyceride, total protein and Albumin. Serum iron (Fe), and ferritin.

Serum insulin, Ceruloplasmin, Zn and Cu levels, CRP and lipocalin-2 (Lcn2) .

Statistical analysis

All data will be analyzed with Statistical Package for the Social Sciences version 20 software (SPSS, Inc., Chicago, IL). Results will be displayed as mean ± SD. Paired Student's t-test used to compare the data pre-operative and nine months postoperative. The chi-squared test used for category variables. Spearman correlation coefficient used to detect the correlation between different variables. Statistical correlations calculated by Pearson's correlation test. P \< 0.05 is considered significant.

02

Conditions studied

  • Nutritional Disorder

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Keywords

  • obesity
  • zinc
  • copper
  • lipocalin 2
03

In context

Nutrition Disorders

275 studies on the registry are indexed under Nutrition Disorders; 31 are open to participants now.

This study's enrollment of 107 is close to the median of 108 across 74 observational studies indexed under Nutrition Disorders.

Browse Nutrition Disorders studies →

Lead sponsor

Alexandria University is the lead sponsor of 569 studies on the registry; 125 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

adult obese subjects with BMI above 40 both males and females presence of obesity comorbidities as hypertension, insulin resistance "type 2 DM" eligible for laporoscopic sleeve gatrectomy

Inclusion criteria

  • micronutrient deficiency in morbid obese subjects Adults.
  • BMI above 40
  • presence of comorbidities as hypertenion, DM, dislipidemia

Exclusion criteria

Exclusion Criteria:

  • all causes which might cause micronutrient deficiency as presence of gastroesophageal reflux
  • all causes which may cause increase obesity "BMI" as hormonal disturbance ; hypothyroidism or cushing, females receiving contraceptive pills
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
107 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Preoperative Clinical characteristics and metabolic biomarkers

    BMI and biochemical parameters including trace elements in patients undergoing laparoscopic sleeve gastrectomy before surgery

    Procedure: laparoscopic sleeve gastrectomy

  • 9 months' Postoperative metabolic biomarkers

    BMI and biochemical parameters including trace elements in patients 9 months after laparoscopic sleeve gastrectomy

    Procedure: laparoscopic sleeve gastrectomy

Interventions

  • Procedurelaparoscopic sleeve gastrectomy

    bariatric surgery to loss weight

06

What researchers measure

Primary outcomes

  1. Evaluation of zinc to copper ratio as biomarker of micro-nutrient deficiency

    detect if there are micronutrient deficiency in morbid obesity in form of zinc to copper ratio and re-evaluate it after loss of weight

    Time frame: nine months

Secondary outcomes

  1. correlate zinc to copper ratio to lipocalin 2 and other metabolic biomarkers

    zinc to copper ratio is considered as biomarker of micronutrient status; therefore, it is correlated it with BMI, other biomarkers of inflammation (lipocalin 2) and other parameters as BMI, FBG to determine if micronutrient status improve after weight loss or not

    Time frame: nine months

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Yerlikaya FH, Toker A, Aribas A. Serum trace elements in obese women with or without diabetes. Indian J Med Res. 2013 Feb;137(2):339-45. PubMed 23563378 ↗

Study documents

  • Protocol and statistical analysis plan · Sep 13, 2020
  • Informed consent form · Sep 13, 2020

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04554082
Lead sponsor
Alexandria University
Responsible party
hala mourad demerdash (Consultant Clinical Pathology, Alexandria University) — Principal investigator
First posted
Sep 18, 2020
Start date
Jan 1, 2015
Primary completion
Jan 1, 2020
Completion
Apr 1, 2020
Last update
Sep 18, 2020

Study contacts

Hala M Demerdash, MD
principal investigator · Alexandria University Hospitals

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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