PeriodontitisOral Health Quality of Life (OHQoL) Was Assessed
Investigational drug(s) / intervention(s)
Non Surgical Periodontal Therapy
Non Surgical Periodontal Therapy: Full mouth subgingival instrumentation will be done
Study summary
The distribution- and anchor-based methods will be used to estimate the Minimal Important Difference (MID) of the OHIP-P-HIN. Two established distribution-based approaches, the standardized effect size (ES) and standardized response mean (SRM) will be calculated. The ES is calculated by dividing the mean change scores in the OHIP-P-HIN from baseline by the standard deviation of the baseline scores. And the SRM are computed as ratios of the mean change score divided by its standard deviation. The anchor-based approach will be applied by using the global transition scale as the anchor.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* ≥18 years of age
* patients able to understand and complete questionnaires independently
* confirmed diagnosis of periodontitis
Exclusion Criteria:
* Patients with systemic diseases such as acquired immunodeficiency syndrome or diabetes mellitus
* pregnancy
* required prophylactic antibiotic coverage prior to dental treatment,
* patients with bleeding disorders
* patients who had received non-surgical periodontal therapy within the preceding eight weeks.
Primary outcome measure(s)
Minimal Important Difference (MID) — 6 weeks after completion of Non surgical Periodontal therapy The distribution- and anchor-based methods will be used to estimate the MID. Two established distribution-based approaches, the standardized effect size (ES) and standardized response mean (SRM) will be calculated. The anchor-based approach will be applied by using the global transition scale as the anchor.
Trial sites (1)
Facility
City
Region
Status
PGIDS Rohtak
Rohtak
Haryana
Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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