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Individualized Homoeopathy as adjuvant therapy to nonsurgical periodontal treament in patients with chronic periodontitis

Individualized Homoeopathy as adjuvant therapy to nonsurgical periodontal treament(NSPT)in patients with chronic periodontitis:A randomized double arm comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/026254
Enrollment
110
Registered
2020-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K053- Chronic periodontitis

Interventions

Intervention1: Individualized Homoeopathic Medicine,Standardized Allopathic medicine : After Randomization standardized Non surgical periodontal treatment (NSPT) will be given to all the subjects by D

Sponsors

DrVHDave Homoeopathic Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between 10 to 70 years of both sexes. 2.Presenting/Diagnosed with chronic periodontitis with 3.Presence of at least 6 natural teeth. 4.Diagnosed cases of periodontitis without previous homoeopathic treatment in the last 1 month.

Exclusion criteria

Exclusion criteria: 1.Cases of severe periodontitis (more than 5 mm CAL) which require surgical interventions by dentist. 2.Known cases of serious systemic disease (HIV etc.) or on-going infectious disease (TB, infectious mononucleosis etc.) 3.Antibiotic & steroid therapy for periodontitis or gingivitis or any other condition in last 1 month. 4.Patients who have undergone nonsurgical periodontal treatment (NSPT) within 6months. 5.Patients on anti-thrombotic treatment (heparin, antivitamin K). 6.Pregnant and breastfeeding mothers 7.Alcoholics. 8.Smokers/Regular tobacco chewers 9.Patients using orthodontic appliances 10.Cases having severe oral inflammation unrelated to periodontal conditions. 11.Cases requiring immediate tooth extraction.

Design outcomes

Primary

MeasureTime frame
Primary outcomes- Clinical attachment loss (CAL in mm) at baseline, 1st , 3rd , 6th and 9th month Timepoint: 00-03 month Enrollment of the cases. (3 months)—

Secondary

MeasureTime frame
1 Probing pocket depth (PPD in mm) at baseline,1st, 3rd, 6th and 9th month 2 Visible plaque index (VPI in 0-3 grade) at baseline,1st, 3rd , 6th and 9th month 3 Presence or absence of Bleeding. Bleeding index (BI) at baseline,1st , 3rd , 6th and 9th month 4 Calculus Index (CI) at baseline,1st, 3rd, 6th and 9th month 5 X RAY findings/ Orthopantomogram (OPG) at baseline (where CAL â?¥ 4 mm was present) and at end of treatment 6 Oral Health Assessment Tool at baseline and end of treatment. Timepoint: 03-12 month Follow up the cases. (9 months)—

Countries

India

Contacts

Public ContactDrLeena Dighe

Dr.V.H.Dave Homoeopathic Medical College

scan28387@gmail.com09979878049

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026