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Lead PoisoningNCT05744752

Effects of Allium Sativum and Moringa Oleifera Extract on Dental Enamel

A study testing Lead Acetate, Moringa oleifera Extract and Allium sativum Extract in people with Lead Poisoning, run by Arslan Saleem at 1 site in Pakistan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Primary objective is to observe the effects of lead on dental enamel of rabbit by measuring; Structural and morphological change by SEM, AFM Elemental composition by SEM-EDX Molecular composition and hydroxyapatite crystal changes by Raman Spectroscopy Blood parameters by serum analysis Secondary objectives includes… Read more about this study

Who is it for?
Ages 3 months to 5 years, men only
Conditions the study is for
Lead Poisoning
What is being tested?
Lead Acetate, Moringa oleifera Extract and Allium sativum Extract
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
90 participants
Where
1 sitePakistan
Study dates
19 Dec 2022to Aug 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 months to 5 years
  • Men only
  • No healthy volunteers
  • Child

Who may be able to join

  • Healthy rabbits
  • Rabbits Age 9-10 weeks
  • Weight 1000-1200 g will be selected

Who cannot join

  • Diseased rabbit
  • Age: More than 10 weeks and less than 9 weeks
  • Weight more than 1200 g and less than 1000 g

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Baqai Medical University

    Karachi, Sindh, 75340

Other trials in Pakistan

About this study

Official title: Protective Effects of Allium Sativum and Moringa Oleifera Extract in Alleviating Lead Induced Defects on Dental Enamel of Rabbits

Primary objective is to observe the effects of lead on dental enamel of rabbit by measuring;

  • Structural and morphological change by SEM, AFM
  • Elemental composition by SEM-EDX
  • Molecular composition and hydroxyapatite crystal changes by Raman Spectroscopy
  • Blood parameters by serum analysis Secondary objectives includes
  • To compare the protective effects of Allium sativum and Moringa oleifera on dental enamel defects due to lead
  • To determine the beneficial effects of AS and MO extract in remineralization of dental enamel.
Read the detailed description

This Animal experimental study will be carried out in animal House, University of Health Sciences, Lahore (UHS) and COMSATS University, Lahore. For this study fifty four healthy male, white NewZeeland rabbits (9 to 10 weeks) will be taken for the study. Rabbits will be randomly divided into 6 groups. Sample size will be 9 rabbits in each group. Experimental animals will be assigned number 1,2,3,4, till 54 using the random number generator and the randomly divided into six groups (n=9) and will be assigned as group A, B, C, D, E, and F. Healthy male, white New Zeeland rabbits weighing 1000-1200 grams (Age 9-10 weeks) will be selected from University of Veterinary and Animal Sciences, Lahore. The animals will be shifted to animal house of UHS. Animals will be kept in experimental research laboratory at controlled room temperature (22-24°C) and humidity (45-65 %) under 12/12 hours natural light and dark cycle for 2 weeks to acclimatize in new environment. All experimental animals will be fed on vegetables, fruits and distilled water ad libitum. At the end of 12 weeks, all the animals will be sacrificed under deep anesthesia. Ketamine hydrochloride 45 mg/kg b.w and xylazine 5 mg/kg b.w I/M will be given to maintain deep anesthesia. Afterwards, 20 mg xylazine was injected into the pinna vein to sacrifice the rabbits while they were anesthetized.(35).

Blood Sampling: The Central Auricular Artery(36) or lateral saphenous vein will be selected to collect 4 ml blood on day 0, after 8 weeks and at the end of 12 weeks. The sample will be collected in serum separating tube for investigations like blood lead count, alkaline phosphatase, calcium and phosphate level.

Tissue Sampling Technique:

A portion of 4x5 mm2 from middle third of crown labial surface will be taken for investigations. The cutting will be done by diamond disc and high speed turbine with irrigation of water to ovoid over heating of sample. Right mandibular incisors of all the rabbits will be selected for SEM and AFM. The left mandibular incisors of all the rabbits will be selected SEM-EDX and RMS analysis. All samples will be labeled and stored in sterilized container having 12% formalin for 72 hours.

Laboratory Processing:

  1. Scan Electron Microscopy: Right mandibular incisor will be selected for SEM analysis. The structure and morphological features of enamel will be seen by its images. The sample will be washed with distilled water and will be dried by hot air blower at slow speed. Sixteen samples can be fixed on a sample stab at a time. Samples will be fixed on stab by double copper tape. The exposed stab will also be covered by copper tape and only the sample part will be left uncovered. Gold coating will be done in sputter coater machine to make the surface conductor for fine details of images. The sample stab will be place in sputter machine chamber and lid will be closed. Inside the chamber, vacuum will be created and argon gas will be filled. Potential of 40 volts will be given. By this plasma will be formed inside the chamber and the electrons of argon gas will strike on gold plate. The tiny gold particles will start sputtering on sample stab. Once gold coating will be done, the procedure will be reversed. The chamber will be filled with air and lid will be opened. Now the sample will be processed in NOVA NANOSEM 450 for ultrastructural details.
  2. Energy Dispersive Spectroscopy: EDX will be used to study elemental composition of mineral contents. A detector of OXFORD X-ACT, PENTA FET will be attached with NOVA NANOSEM 450. The same sample used for SEM will also be used for SEM-EDX analysis. This will give details on the surface up to 2 micron thickness.
  3. Atomic Force Microscope: AFM (SPM-9500J3, Shimadzu Corp, Japan) will be used for the assessment of morphological features of enamel surface. It provides the three-dimensional surface topography without any sample preparation. This microscopy is designed to scan the sample with a probe. Sample will be attached on stub, which will be fixed and manually adjusted. Laser adjustment will be done after determining probe frequency. Finally, scanning and image processing will be done with WinSPM system processing. For one representative sample, micrographs at six different areas (2.0×2.0 μm scan area) will be taken using AFM (SPM-9500J3, Shimadzu Corp, Japan) and AFM software (SPM-Offline, Shimadzu Corp, Japan). AFM creates 3D images of a surface by scanning a micron-size cantilever across the surface, which is typically made of silicon or silicon nitride, with a tip whose radius of curvature is ~10nm. The cantilever is deflected by the forces between the tip and the surface, which are ~nN and include contributions from electrostatic forces, solvation forces, Vander Waals interactions, and chemical bonding. This deflection of cantilever is measured by a laser spot reflecting from the top surface of the cantilever into an array of photodiodes, which provides images on the computer.
  4. Raman spectroscopy: It is a non-destructive chemical analysis technique which provides detailed information about chemical structure, crystallinity and molecular interactions. The RMS will give us the details of the entire thickness of enamel about the molecular composition and its interaction of the sample. No special sample preparation will be needed for this analysis and the sample can also be used for other investigations. InVia Raman Microscope by RENISHAW UK will be used for this study. The laser intensity 488nm will be used for 10 seconds. The RMS will be done on 6 different spots and the average reading will be used in study.
Conditions
Lead Poisoning
Being tested
Lead Acetate, Moringa oleifera Extract, Allium sativum Extract, Placebo
Keywords
Moringa oleifera extract, Allium sativum extract, Dental Enamel, Rabbits
Medical subject headings
Lead Poisoning

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lead AcetateOther

    The oral LD50 of lead acetate is 390mg/kg body weight. The experimental group B, C, and D will receive a single dose of 19.5 mg/kg b.w (1/120th of LD50),31 daily dissolved in distilled water and given by oral gavage method for 12 weeks. Lead acetate Pb(CH3COO)2x3H2O, will be purchased from Sigma-Aldrich Chemie (Germany).

  • Moringa oleifera ExtractDietary supplement

    The method described by Hanaa Elgamily(32) with minor modifications. Fresh Leaves will be washed and dried in dry heat oven. All the preparation will be done in pharmacological department, University of Health Sciences in sterile environment. Dried leaves will be crushed to make fine powder. 1000 g powder of MO will be socked in 5000 ml of 70% ethanol (70% ethanol and 30% distilled water) for 72 hours at room temperature. Then mixture will be magnetically stirred for 24 hours and stored at 4oC for 48 hours to allow extraction of active ingredients. Then the mixture will be filtered twicely by using Whatman No 1 filter paper. The extract will be concentrated by rotary vacuum evaporator at 40 oC to evaporate the solvent. The extract will be freeze, dried and stored at -70 oC for use. Dose of MO extract will be 400 mg per kg.(33) body weight given daily in 1ml of distilled water by oral gavage method for 12 weeks.

  • Allium sativum ExtractDietary supplement

    Fresh Allium sativum bulbs will be selected for study. The cloves will be peeled, washed with distilled water and dried under shed. Then it will be chopped into small pieces. 1000g of chopped garlic will be crushed by mortar and passel. The garlic paste will be mixed with 5000 ml of 70% ethanol (70% ethanol and 30% distilled water) for 72 hours at room temperature. Rest the procedure is same as mentioned in moringa extract. Dose of 500 mg per kg(34) body weight garlic extract will be given daily in 1ml of distilled water.

  • PlaceboOther

    1ml NaCl 0.9% daily for 12 weeks

Study groups in NCT05744752
Study groupRoleWhat they receive
Group AOtherControl; Placebo 1ml NaCl 0.9% daily for 12 weeks
Receives: Other: Placebo
Group BActive comparatorPb Group; Lead acetate 19.5mg/kg b.w daily for 12 weeks
Receives: Other: Lead Acetate
Group CExperimentalPb + Allium sativum extract; Lead acetate 19.5mg/kg b.w followed by Allium sativum(AS) extract 500 mg/kg b.w daily for 12 weeks
Receives: Other: Lead Acetate; Dietary Supplement: Allium sativum Extract
Group DOtherCPb + Moringa oleifera extract; Lead acetate 19.5mg/kg b.w followed by Moringa oleifera extract 400mg/kg b.w daily for 12 weeks
Receives: Other: Lead Acetate; Dietary Supplement: Moringa oleifera Extract
Group EActive comparatorAllium sativum extract; Allium sativum extract 500mg/kg b.w daily for 12 weeks
Receives: Dietary Supplement: Allium sativum Extract
Group FExperimentalMoringa oleifera extract; Moringa oleifera extract 400mg/kg b.w daily for 12 weeks
Receives: Dietary Supplement: Moringa oleifera Extract

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Histological Outcomes

    In this examination Odontoblastic zone, Cell nuclei Vacuolization of odontoblasts, Acute Inflammation, Chronic Inflammation, Apatite formation, Collagen crosslinking will be determined inform of normal or abnormal.

    Measured: at the end of the study

Secondary outcomes (1)
  1. Mineral Concentration

    Mineral concentration like Ca/P etc. ratio will be assessed by SEM \& EDX analysis

    Measured: at the end of the study

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Feb 2023
  2. Study start19 Dec 2022
  3. Primary completionMay 2023 (estimated)
  4. Study completionAug 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Factorial
Model description
A total of 90 male rabbits of average weight 1-2 kg will be obtained from the animal house of COMSATS University, Lahore. These rabbits will be segregated into 06 groups, each group consisting of 15 rabbits. All rabbits will be kept safe in iron cages under controlled temperature (25±2 C), humidity (55 ± 5%), and 12-hour dark-light cycle. One week after their acclimatization into a new environment the trial will begin. All experimental protocols will be performed following the guidelines for the human use of laboratory animals established at COMSATS University, Lahore.
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05744752
Sponsor's protocol ID
Trial2022001
Status last verified
Feb 2023
First submitted
17 Oct 2022
Last updated
27 Feb 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data analysis will be presented in the form of graphs and tables in the thesis. The graphs will be generated from Energy-dispersive X-ray spectroscopy(EDX) and Scanning Electron Microscope (SEM) and will interpreted by the Expert.

Publications

  • Du Toit N, Kempson SA, Dixon PM. Donkey dental anatomy. Part 2: Histological and scanning electron microscopic examinations. Vet J. 2008 Jun;176(3):345-53. doi: 10.1016/j.tvjl.2008.03.004. Epub 2008 Apr 18.

    PubMed 18396075
  • Six N, Lasfargues JJ, Goldberg M. Differential repair responses in the coronal and radicular areas of the exposed rat molar pulp induced by recombinant human bone morphogenetic protein 7 (osteogenic protein 1). Arch Oral Biol. 2002 Mar;47(3):177-87. doi: 10.1016/s0003-9969(01)00100-5.

    PubMed 11839353
  • Yu C, Abbott PV. An overview of the dental pulp: its functions and responses to injury. Aust Dent J. 2007 Mar;52(1 Suppl):S4-16. doi: 10.1111/j.1834-7819.2007.tb00525.x.

    PubMed 17546858

Questions about this trial

What is this clinical trial studying?

A study testing Lead Acetate, Moringa oleifera Extract and Allium sativum Extract in people with Lead Poisoning, run by Arslan Saleem at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 27 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Histological Outcomes (time frame: at the end of the study). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05744752, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Feb 2023; AzTrials last refreshed its copy on 8 Nov 2026.

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