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Register:	ClinicalTrials.gov
Last refreshed on:	12 October 2015
Main ID:	NCT02127346
Date of registration:	25/04/2014
Prospective Registration:	Yes
Primary sponsor:	Damascus University
Public title:	Relationship Between Chronic Periodontitis and Vitamin D and Calcium in Men
Scientific title:	Relationship Between Chronic Periodontitis and Vitamin D and Calcium in Men
Date of first enrolment:	May 2014
Target sample size:	200
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT02127346
Study type:	Observational
Study design:	Observational Model: Case Control, Time Perspective: Cross-Sectional
Phase:	N/A

Countries of recruitment
Syrian Arab Republic

Contacts

Name:	Rowaida Saymeh, DDS MSc PhD
Address:
Telephone:
Email:
Affiliation:	Professor of Periodontics, Department of Periodontics, University of Damascus Dental School, Damascus

Name:	Suleiman Dayoub, DDS MSc PhD
Address:
Telephone:
Email:
Affiliation:	Associate Professor of Periodontics, Department of Periodontics, University of Damascus Dental School, Damascus

Name:	Mohammad Alharissi, DDS MSc
Address:
Telephone:
Email:
Affiliation:	PhD student, Department of Periodontics, University of Damascus Dental School, Damascus

Key inclusion & exclusion criteria

First group (Chronic Periodontitis) inclusion criteria:

1. Male patients

2. Patients are suffering from chronic periodontitis

3. Patients do no have systemic diseases

4. Patients should have 20 teeth at least

5. 30 year old at least

Second group (Healthy Volunteers) inclusion criteria:

1. Male individuals

2. With no systemic diseases or periodontitis

3. 30 year old at least

4. 20 teeth at least for each participant

Age minimum: 30 Years
Age maximum: 50 Years
Gender: Male

Health Condition(s) or Problem(s) studied

Chronic Periodontitis

Intervention(s)

Primary Outcome(s)

Serum Vitamin D concentration [Time Frame: One time assessment, within 24 hours before delivering any treatment]

Serum Calcium concentration [Time Frame: One time assessment, within 24 hours before delivering any treatment]

Secondary Outcome(s)

Bleeding on Probing [Time Frame: One time assessment once sample recruitment has completed and within 24 hours before delivering any treatment.]

Clinical Attachment Loss (CAL) [Time Frame: One time assessment once sample recruitment has completed and within 24 hours before delivering any treatment.]

Pocket Depth [Time Frame: One time assessment once sample recruitment has completed and within 24 hours before delivering any treatment.]

Secondary ID(s)

UDDS-Perio-04-2014

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:
Date Posted:
Date Completed:
URL:

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