A study to assess the effectiveness of a 1 percentage feracrylum solution delivered into gums as the treatment of gum disease

To evaluate the efficacy of a 1 per cent feracrylum solution as local drug delivery in treating chronic periodontitis A randomised control trial. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/07/114098

Enrollment

Registered

2026-07-15

Start date

Unknown

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

None listed

Interventions

Intervention1: Feracrylum group: one percent feracrylum solution locally delivered into the periodontal pocket of test group after scaling and root planing at baseline Control Intervention1: placebo g

Eligibility

Inclusion criteria

Inclusion criteria: patients between 30 and 70 years of age having chronic periodontitis pocket depth greater than 5 mm and clinical attachment loss greater than 4 mm are included

Exclusion criteria

Exclusion criteria: pregnant and lactating women and smokers patients under steroids or other immunosuppressants and patients with systemic diseases like diabetes mellitus are excluded

Design outcomes

Primary

Measure	Time frame
Clinical attachment levelTimepoint: At baseline one month and 3 months	—

Secondary

Measure	Time frame
gingival index probing pocket depthTimepoint: baseline 4 weeks and 8 weeks	—

Countries

India

Contacts

Public ContactDR DEBOPRIYA CHATTERJEE

RUHS COLLEGE OF DENTAL SCIENCES

banerjee.debo@gmail.com7568677717

Outcome results