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Evaluation of 2%Bromelain Gel With 0.2%CHX Gel as Subgingival LDD Following SRP in Stage II/III and Grade B Periodontitis -A RCT

K

Krishnadevaraya College of Dental Sciences & Hospital

Status and phase

Enrolling
Phase 1

Conditions

Periodontal Pocket

Treatments

Procedure: SRP
Drug: Bromelain gel
Drug: chlorhexidine gel

Study type

Interventional

Funder types

Other

Identifiers

NCT06505759
02-D012-147453

Details and patient eligibility

About

The current study is a prospective randomised study Evaluation of 2%Bromelain Gel With 0.2%Chlorhexidine Gel as Subgingival Local Drug Delivery Following Scaling and Root Planing in Stage II/III and Grade B Periodontitis

Full description

36 sites with periodontal pocket depth measuring 4-6mm were selected. The sites selected were divided into

  1. Group I (Control)- 12 sites with Probing depth of ≥5mm treated with scaling and root planing alone.
  2. Group II -12 sites with Probing depth of ≥5mm treated with scaling and root planing followed by placement of bromelain gel.
  3. Group III -12 sites with Probing depth of ≥5mm treated with scaling and root planing followed by placement of chlorhexidine gel.

periodontal pack was placed and patient was recalled at 1week,4th week and 12th week

Enrollment

36 estimated patients

Sex

All

Ages

30 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patient with have chronic periodontitis in the age group between 30-50 years.

  • Patients having ≥20 teeth.

    -.Patients with radiographic evidence of bone loss in atleast two teeth.

  • Patients who are systematically healthy.

  • Patients with localized pockets with probing depth of ≤ 5mm.

  • Patients who are cooperative and able to attend the hospital for regular follow-up.

Exclusion criteria

  • Patients who have received any surgical or nonsurgical therapy during past 6months
  • Pregnant or lactating females.
  • Use of systemic antibiotics in the past 6 months.
  • Patient who are not willing to give a written informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 3 patient groups

GROUP 1-SRP alone
Active Comparator group
Description:
control group is treated with SRP alone
Treatment:
Procedure: SRP
GROUP 2-0.2% BROMELAIN gel
Experimental group
Description:
test group is treated with bromelain gel
Treatment:
Drug: Bromelain gel
GROUP 3-0.2% CHLORHEXIDINE gel
Active Comparator group
Description:
test group is treated with chlorhexidine gel
Treatment:
Drug: chlorhexidine gel

Trial contacts and locations

1

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Central trial contact

DR.NALLAGATLA VAMSI VENKATAKRISHNA SAI, MDS; DR .Prabhuji MLV, MDS

Data sourced from clinicaltrials.gov

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