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Hormonal Status and Quality of Life in Female Postmenopausal Patients With Burning Mouth Syndrome

NCT04535973 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2020-09-02

No results posted yet for this study

Summary

The aim of this study was to determine the level of salivary estradiol, progesterone and dehydroepiandrosterone in female postmenopausal women with and without burning mouth syndrome. In all participants the quantity of unstimulated and stimulated saliva would be determined and they would fulfill self-perceived quality of life questionnaire Oral Health Impact Profile-14 (OHIP-14). Intensity of burning symptoms would be determined on visual-analogue scale grading 0-10. All data would be compared between study and control group.

Conditions

  • Burning Mouth Syndrome
  • Progesterone
  • Dehydroepiandrosterone
  • Quality of Life
  • Hormone Disturbance
  • 17β-Estradiol

Interventions

DIAGNOSTIC_TEST

unstimulated saliva sample for hormone analysis

hormone levels will be determined in frozen samples of unstimulated saliva

OTHER

quality of life questionnaire

all participants will fill out self-perceived quality of life questionnaire

Sponsors & Collaborators

  • University of Zagreb

    lead OTHER

Eligibility

Min Age
51 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-11-15
Primary Completion
2020-06-15
Completion
2020-06-15

Countries

  • Croatia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04535973 on ClinicalTrials.gov