Skip to main content
Clinical Trials/CTRI/2019/09/021214
CTRI/2019/09/021214
Not yet recruiting
未知

Assessment and comparison of bone marker levels and bone density in PCOS subjects with or without Chronic Periodontitis before and after non surgical periodontal therapy - PCOS-CP

SERB DST0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: R888- Abnormal findings in other body fluids and substancesHealth Condition 2: E282- Polycystic ovarian syndrome
Sponsor
SERB DST
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
SERB DST

Eligibility Criteria

Inclusion Criteria

  • Women between 18 and 30 years of age.
  • 2\. PCOS diagnosis will be based on the criteria by Rotterdam2 with the presence of at least two of the following: polycystic ovaries, oligomenorrhea and/or anovulation, hyperandrogenism (clinical and/or biochemical)
  • 3\. Diagnosis of generalized moderate\-to\-severe chronic periodontitis will be based on presence of at least 20 teeth in the oral cavity, with at least 30% of the areas undergoing clinical attachment loss of at least 3 mm and a probing depth of \>\=5 mm and radiographic evidence of bone loss3\.
  • 4\. The systemically healthy group will be based on; history of regular menstrual cycles, no clinical or biochemical sign of hyperandrogenism, matching with the PCOS group in body mass index (BMI) and exclusion of PCOS by ultrasound examination.
  • 5\. Willingness to sign consent for study including participation with collection of blood specimens
  • 6\. Willingness to discontinue OCP for duration of study period up to 18 weeks

Exclusion Criteria

  • 2\. History of smoking or any drug usage, including oral contraceptives, systemic antibiotics (during the previous 6 months) or continuous use of NSAIDs
  • 3\. History of any dental treatment in the previous six months.

Outcomes

Primary Outcomes

Not specified

Similar Trials