The Effect of Non-surgical Periodontal Therapy Plus Doxycycline on HbA1c in Patients With Type 2 Diabetes Mellitus
The Effects of Non-surgical Periodontal Therapy Plus Doxycycline on HbA1c in Patients With Type 2 Diabetes Mellitus: A Randomized Clinical Trials
1 other identifier
interventional
24
0 countries
N/A
Brief Summary
Aim: The purpose of this study is to investigate the effect of nonsurgical periodontal therapy plus doxycycline on glycemic control in type 2 diabetes mellitus (type 2 DM) patients who have periodontitis. Materials and methods: A total of 24 type 2 DM patients with periodontitis will be selected for the study, and randomly divided into two equal groups,who are at least 35 years of age and 16 teeth and type II diabetes are (at least the last 3 months of diagnosis of diabetes and its FBS More than 110 have), and also with periodontal disease are chronic moderate (at least in three areas Attachment level to a depth of 3-4 mm maxillary or mandibular been confirmed by clinical examination and radiographic signs are being); Takes place. The initial HbA1c Patients should be between 7-9 percent over the past three months has changed his medication also found the necessary explanations on how to do that consent, Plaque index (PI) by Loe \& Silness, bleeding on probing (BOP) based on Carter and Barnes (if any bleeding number 1 and its absence is 0), probing depth (PD) and clinical attachment levels (CAL) were recorded. "Group 1": (12 patients) was treated with oral hygiene instruction, Scaling, and root planing, and doxycycline for 15 days; and "Group 2": (12 patients) has the same treatment but with placebo, After 12 weeks their periodontal condition and Fasting blood sugar (FBS), glycated hemoglobin (HbA1c) level, will be reevaluated.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2014
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedFirst Submitted
Initial submission to the registry
May 24, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2016
CompletedFirst Posted
Study publicly available on registry
July 26, 2016
CompletedOctober 4, 2016
September 1, 2016
1.2 years
May 24, 2016
September 30, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
Periodontal pocket depth
Periodontal Probes Measuring (millimeters)
15 days
Secondary Outcomes (1)
glycated hemoglobin (HbA1c)
3 months
Study Arms (2)
oral doxycycline
ACTIVE COMPARATOROral capsules of doxycycline 100 mg were used
oral placebo capsule
PLACEBO COMPARATORoral placebo capsule were used
Interventions
Oral doxycycline 100mg was taken within 15 days
Eligibility Criteria
You may qualify if:
- Patients with diabetes mellitus type II (at least 3 months before diagnosis, and A fasting blood sugar level of more than 125 mg/dl) and has periodontal disease is a chronic moderate (has a clinical attachment level of 3-4 mm) peritonitis
- Minimum of 16 natural teeth, and no periodontal treatment in the prior 6 months, - Had a glycated α hemoglobin (HbA1c) value between 7- 9 percent at screening
- Had reported no changes in diabetes medications within the last 3 months were in the care of a physician for their diabetes.
You may not qualify if:
- Pregnancy or lactation
- History of allergy to drugs used in the study
- Smoking
- Diabetes-related emergency within 30 days ago
- Use of nonsteroidal anti-inflammatory drugs
- Or taking low dose daily aspirin (75-325 mg)\\
- Use of immunosuppressive medications; antibiotic use
- Dialysis
- Risk of bleeding complications
- The type of disease periodontal (Aggressive)
- A history of periodontal treatment in the previous 6 months
- Orthodontic treatment
- Using the removal prostheses
- Extensive dental caries
- Dental abscesses or infections.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- assistant prof
Study Record Dates
First Submitted
May 24, 2016
First Posted
July 26, 2016
Study Start
September 1, 2014
Primary Completion
December 1, 2015
Study Completion
July 1, 2016
Last Updated
October 4, 2016
Record last verified: 2016-09
Data Sharing
- IPD Sharing
- Will share