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Diabetes (DM)NCT07858604

Awareness of Bidirectional Relation of Diabetes Mellitus and Periodontal Health

An observational study of Diabetes (DM), run by Cairo University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record

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Trial summary

The study will recruit patients having diabetes mellitus; where they will be asked to answer a questionnaire after obtaining an informed consent. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Diabetes (DM)
What is being tested?
Questionnaire and Physical Exam
Type of treatment
Pill or oral medicine
How many people
323 participants
Where
No sites listed yet
Study dates
Oct 2026to Nov 2027
Phase
Observational

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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients with diagnosed Diabetes Mellitus

Who may be able to join

  • 1. Patients with Diabetes Mellitus aged 18 years old and more. 2. Patients willing to participate in the study.

Who cannot join

  • 1. Patients refusing to participate in the study. 2. Handicapped patients.

About this study

Official title: Patient Awareness, Perceived Barriers, and Educational Needs Regarding the Bidirectional Relationship Between Periodontitis and Diabetes Mellitus Patients: A Cross Sectional Questionnaire Study

The study will recruit patients having diabetes mellitus; where they will be asked to answer a questionnaire after obtaining an informed consent.

Read the detailed description

A structured, self-administered questionnaire was developed specifically for this study based on an extensive review of the relevant literature on diabetes mellitus and periodontal disease awareness. The questionnaire consists of six main sections: (A) Socio-demographic information, (B) Diabetes-related information, (C) Oral health status and practices, (D) Awareness of the bidirectional relationship between diabetes and periodontal disease, (E) Perceived barriers to oral healthcare, and (F) Educational needs.

Conditions
Diabetes (DM)
Being tested
Questionnaire and Physical Exam
Medical subject headings
Diabetes Mellitus

What participants receive

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

  • Questionnaire and Physical ExamOther

    The questionnaire consists of six main sections: (A) Socio-demographic information, (B) Diabetes-related information, (C) Oral health status and practices, (D) Awareness of the bidirectional relationship between diabetes and periodontal disease, (E) Perceived barriers to oral healthcare, and (F) Educational needs.

Study groups in NCT07858604
Study groupRoleWhat they receive
Diabetic patientspatients having diabetes mellitus
Receives: Other: Questionnaire and Physical Exam

What is being measured

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

  1. The awareness of the bidirectional link between diabetes and periodontal disease among diabetic patients.

    questions to identify the awareness of the bidirectional link between diabetes and periodontal disease among diabetic patients.

    Measured: 2 months

Secondary outcomes (1)
  1. 1- The perceived barriers that prevent diabetic patients from receiving periodontal treatment. 2- The educational needs for diabetic patients to receive periodontal treatment.

    questions within the questionnaire to identify these outcome measures

    Measured: 2 months

Timeline

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

  1. First posted5 Oct 2026
  2. Study startOct 2026 (estimated)
  3. Primary completionOct 2027 (estimated)
  4. Study completionNov 2027 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case only
Time perspective
Cross-sectional
Enrolment
323 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07858604
Sponsor's protocol ID
ACU-Per5
Status last verified
Sep 2026
First submitted
29 Sep 2026
Last updated
5 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

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